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Career postings for the Massachusetts Biotechnology Council

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  • 11/12/15--22:19: Senior Data Architect
  • Company Background

     

    Aegerion Pharmaceuticals is a biopharmaceutical company dedicated to the development and commercialization of innovative, life-altering therapies for patients with debilitating rare diseases.

    At Aegerion, we believe that our employees are our strongest asset. We strive to recruit high performing, best-in-class candidates who possess a proven track record of success. We seek candidates who are patient-centric, passionate, entrepreneurial-minded, and interested in joining a high caliber and collaborative team. Our culture offers a kind, energetic, high-growth, and fun environment that provides an unmatched opportunity for individual contribution and development. We emphasize the ability to make an indelible difference within the organization and in the lives of our patients. Aegerion’s headquarters are in Cambridge, MA, and the company trades on the NASDAQ Stock Exchange under the ticker: AEGR.

     

    Position Description

     

    Reporting to the Associate Director of Business Technology, the Senior Data Architect will be a key member of the Commercial/Medical IT team, with a primary focus of planning the data architecture, managing the systems, integration and data feeds related to data governance.  In this position, the incumbent will possess a keen understanding of the Aegerion patient journey and manage all aspects of data governance – customer master, data dictionaries, data modelling, database design, database administration, data integration with vendors/customers and quality of data that is loaded into the Data Warehouse.

     

    The position is located in our Cambridge-based home office, with some limited travel to support business needs.

     

    Key Responsibilities

    • Partner with Global Commercial Operations and medical leadership to develop the organizational data integration strategy
    • Direct and oversee the Master Data Management process for the commercial and medical organizations, including internal rosters, customer master, data dictionaries, etc…
    • Work with Compliance to ensure all requirements are addressed and maintained as part of the overall data governance process.
    • Manage the ongoing Data Warehousing build and maintenance project, working to ensure the flow of data, data quality, and overall data governance is maintained across the organization.
    • Design and Development Schema, Aggregations, Indexes, SQL, Stored Procedures
    • Design database structures & use data modelling tools
    • Develop and support shell scripts for database activities, such as data loading and unloading
    • Develop ETL integration processes between operational systems and enterprise data warehouse
    • Create comprehensive daily system checks to ensure data quality
    • Monitor SQL server databases to ensure optimum performance, analysing and resolving performance issues ensuring maximum uptime
    • Implement and maintain security policies and best practices
    • Ensure backup and recoverability of all enterprise SQL server databases.
    • Responsible for proactive system capacity planning
    • Analyse, translate and develop business requirements into a design of both the metadata and logical data model needed to support both reporting and ad-hoc analysis.
    • Design, build, test and implement data model and reporting solutions
    • Conduct data quality reviews and management reports on the health of the Aegerion data systems and architecture

     

     

    Qualifications and Experience

    • A minimum of five years of experience as a database analyst/administrator in the Life Sciences industry
    • Bachelor’s degree in computer science, or related field, Master’s preferred
    • Strong understanding of pharmaceutical data and data process flows
    • Strong interpersonal, presentation and facilitation skills required
    • Experience with performance monitoring statistics, database optimization, and index utilization.
    • Experience configuring database instances, replication, and show plan utilities.
    • Ability to manage project commitments to ensure that the project comes in on time and within budget.
    • Experience with developing ETL workflows and processes
    • Excellent SQL skills
    • Experience with SQL Server
    • Experience with creating stored procedures and triggers
    • Experience building metadata repositories
    • Experience with OLAP
    • Implementation experience of tools such as Tableau, Crystal Reports, MicroStrategy, BusinessObjects or others
    • Strong relational and multi-dimensional data modeling
    • Excellent analytical skills
    • Ability to effectively present information to internal customers and senior management

     

     Resumes from third party vendors will not be accepted.

    Aegerion Pharmaceuticals is an Equal Opportunity/Affirmative Action Employer: Minorities/Females/Disabilities/Veterans

     


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  • 11/12/15--22:32: Human Neuron Core Manager
  • Supervises and oversees daily operations of the Human Neuron Core, including research assistants working in the Human Neuron Differentiation Service. The Core Manager will create a sustainable business plan for service provision to academic and industry clients requesting human iPSC derived neurons. The core manager will oversee work to create and maintain an organized iPSC repository associated with de-identified patient information. The core manager will identify best practices to develop standard operating protocols for differentiation of specified neuronal cell types that support phenotyping of patient derived iPSC lines. He/She will supervise and train research assistants working in core facility. Oversee supplies and maintenance of equipment and ensures Core’s compliance with hospital and governmental regulations. He/She will works with Directors of Translational Neuroscience Center (TNC) to develop and execute strategies for new target identification and drug repurposing screens using patient derived iPSC neurons. He/She will work with TNC leadership to establish and implement quality control criteria for individual cell types and protocols to support high quality product distribution. Experience with microscopy, high content screening or electrophysiology platforms are an advantage. Experience with CRISPR modification of cell lines is an advantage. Trains and assists users in the use of specialized core equipment, and performs analysis of the data generated to recommend new techniques.

    Requirements:
    Work requires the knowledge of theories, principles, and concepts typically acquired through completion of a Ph.D. in stem cell biology or a closely related field. 5-10 years of experience working in a biopharma, or similar setting, using iPSC lines and/or iPSC-differentiated human neurons is preferred; level will be commensurate with experience. Work requires the analytical skills to resolve complex problems requiring the use of scientific, mathematical, or technical principles and in-depth, experienced-based knowledge. Work requires strong oral and written communication skills to exchange information with interdisciplinary team members, culturally diverse peers and communicate scientific concepts to audiences with varying degrees of scientific background ranging from patients to hospital leadership. This type of interaction requires courtesy and tact when dealing with patients, visitors and/or hospital employees.


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    Summary

    The purpose of this position is to provide a broad range of strategic and tactical insights for the US Sales and Marketing organization through the development of retrospective and prospective analysis and reporting.  Your ability to generate, mine, analyze, and synthesize information related to our products will be critical to the strategic development of product performance.  This position reports to the Vice President, Commercial Operations. 

    Key Responsibilities/Essential Functions

    • Develop complex reporting, forecasts and metrics including: 
    • Compile, analyze, and present sales performance and marketing initiative performance
    • Identify trends, risks, opportunities, and performance both at a product and customer segment level
    • Generation of ROI/IRR analyses for Marketing Programs
    • Support  In Line Product Forecasting including providing price/volume variance analysis
    • Analyze performance versus plan, interpret results, and make recommendations for improvement 
    • Development and maintenance of key customer/competitive intelligence/market repository
      • Perform secondary research to maintain active knowledgebase on market, disease states, key customers and competitors including
        • SEC filings, Annual reports, Earning calls, and press releases
        • Acquire, read, summarize and presentation of appropriate market research reports to constituents
        • Maintain an active pulse on reports issued from relevant associations such as AHA, CDC, Census Bureau, ASE, SNM
        • Support development of analyst/investor presentations with secondary research
    •  Project management efforts will should align with and support the Sales and Marketing teams and may include:
      • Primary/Secondary market research initiatives
      • Product pricing evaluations
      • Customer contract evaluations
      • In depth product reviews
    •  Represent Commercial Analytics by acting as a technical business partner to Business Development efforts.  By leading the coordination of data and analytics as requested, provide insights and support business decision making. 
    • Partner with other functional areas on cross-divisional initiatives to understand overall functioning and the impact on the Sales and Marketing team decision making process.
    • The incumbent will actively promote safety rules and awareness, will demonstrate good safety practices at all times, and take initiative to correct safety hazards.  Additionally, the incumbent will actively demonstrate and promote the Lantheus values of accountability, quality, efficiency, customer service, collaboration, and safety. 

    Basic Qualifications

    • Relevant Bachelor’s degree with a minimum of 15 years of related experience: MBA preferred with a minimum of 10 years experience in market research, marketing analytics, and/or financial analysis.
    • Extensive proven experience with Excel, Access, PowerPoint, SFA (Sales Force Automation), CRM; preferred experience with SQL and VBA
    • Proficient in the use of statistics and other quantitative techniques to evaluate data
    • Proficient in the development of ROI/IRR analyses and other financial evaluation models
    • Proven ability to develop complex models in Excel
    • Proficient in the development of detailed product level market/sales forecast models
    • Demonstrated ability to communicate, write and present analytical summaries to all levels of the organization
    • Detail oriented, self starter with a strong emphasis on teamwork, timeliness, and quality of work

    Other Requirements

    • Maintain current knowledge of, and ensure all work activities are conducted within compliance with the full range of internal and external systems, technology, regulatory requirements and related policies and procedures.

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  • 11/13/15--00:17: Laboratory Coordinator
  • For more information, go to: http://www.cwsciences.com/Current-Openings/Laboratory-Coordinator

     

    Candidates must live local and be a US Citizen or Green Card Holder

    Email resume to: jobs@cwsciences.com

    Commonwealth Sciences is a professional recruiting firm specializing in Science, Engineering and Green Technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors. Our clients value the basic integrity, customer service and industry expertise that defines our organization.

     

    Commonwealth Sciences, Inc.

    www.cwsciences.com


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  • 11/13/15--00:19: Research Assistant
  • For more information, go to: http://www.cwsciences.com/Current-Openings/Research-Assistant

     

    Candidates must live local and be a US Citizen or Green Card Holder

    Email resume to: jobs@cwsciences.com

    Commonwealth Sciences is a professional recruiting firm specializing in Science, Engineering and Green Technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors. Our clients value the basic integrity, customer service and industry expertise that defines our organization.

     

    Commonwealth Sciences, Inc.

    www.cwsciences.com


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    For more information, go to: http://www.cwsciences.com/Current-Openings/Associate-Scientist--Protein-Analytics

     

    Candidates must live local and be a US Citizen or Green Card Holder

    Email resume to: jobs@cwsciences.com

    Commonwealth Sciences is a professional recruiting firm specializing in Science, Engineering and Green Technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors. Our clients value the basic integrity, customer service and industry expertise that defines our organization.

     

    Commonwealth Sciences, Inc.

    www.cwsciences.com


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    E-Commerce Specialist - Salesforce.com CRM & Web Developer
    Skill Level: Intermediate You will support the Head of Leads and Campaigns in the management of leads, including the creation, integration and ongoing maintenance of Salesforce.com-enabled website forms for our public-facing website. You should be familiar with Salesforce.com objects, including Leads, Contacts and Cases. You should have a natural flair for user-focused design, experience in writing custom HTML, CSS, JavaScript and a practical understanding of the latest web technology.
    Role Description:
    * Creation, integration and ongoing maintenance of Salesforce.com-enabled website forms using FormAssembly Enterprise and Intershop (ISH) 7 (CMS) - Web-to-Lead - Web-to-Case - FormAssembly Salesforce.com connectors
    The role requires an independent self-starter capable of working to spec without daily supervision.
    ISH experience a plus (but not necessary). FormAssembly experience an enormous plus.
    Technical Requirements

    Basic understanding of Salesforce.com Objects
    Experience with web development languages of HTML, CSS and JavaScript/jQuery.
    HTML Familiarity of HTML syntax for multiple specifications, including but not exclusive to HTML 5. Familiarity with the semantic markup for display of lists, tabular data, forms, etc. Knowledge of markup used for layout. Knowledge at the level to be able to hand-code markup. CSS How to define, combine and group CSS selectors for HTML elements, ID, classes, pseudo classes, child or sibling. Basic understanding of CSS box model and methods for CSS positioning, absolute and relative. Knowledge of properties and attributes to control display. JavaScript Knowledge of the operators, variables, datatypes, objects, properties and methods. Familiarity with control structures such as objects, functions, conditional statements, arrays, loops and expressions. Forms and regular expression validation and submitting data. Knowledge of how to apply logical operators and conditional statements. Knowledge of the DOM HTML objects and their properties. Familiarity with development and debugging tools for cross-browser issues.


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  • 11/13/15--00:34: Procurement Manager
  • The Category Sourcing Manager - Marketing, Media & Events (MME) - USA/Canada will be responsible for establishing and executing sourcing strategies for a portfolio of Marketing & Communications spend sub-categories in support of multiple affiliates in the USA and Canada, as well as supporting global initiatives. This will be done in collaboration and alignment with the US-based Global Corporate Sourcing Manager, MME and the Germany-based global Head of Procurement Category, MME.
    The role will support the following businesses: EMD Serono (biopharma), EMD Millipore (life sciences), and EMD Inc Canada (biopharma). All are affiliates of Darmstadt, Germany-based Merck KGaA. The selected candidate may be located primarily in Rockland, but may expected to spend time in Billerica locations as requirements dictate.
    As a key link between internal stakeholder departments, Procurement, and EMD’s external supplier base, the Category Sourcing Manager is accountable for understanding key business drivers and ensuring that stakeholder requirements are fulfilled. Extensive cross-functional collaboration, and use of strategic sourcing best practices are keys to maximizing value in terms of cost reduction, risk mitigation, quality and supplier performance. The role holder conducts internal and external spend and market analyses, identifies opportunities, develops category strategies, leads sourcing teams, negotiates contracts and manages key supplier relationships.

    We need an energetic, flexible, outspoken team player capable of forming strong relationships throughout the entire organization. Strong networking skills are a must in order to succeed in this multi-divisional, matrixed organization.

    Key Tasks & Responsibilities
    Broad knowledge of the strategic Marketing, Communications, and Meetings sourcing processes, with the ability to:
    • Influence sourcing strategies/technology within the Marketing and Communications / Media communities
    • Map the supplier landscape for the category, defining improvement plan for near-, mid-, and long-term
    • Perform cost analysis and influence demand for major categories
    • Acquire and maintain a technical understanding of services/products purchased
    • Lead cross functional sourcing efforts relative to supplier selection and qualification
    • Foster teamwork and positive employee relations through regular open communications, problem solving, role modeling and management of relationships
    • Support change across a multi-location environment, including cross functional team facilitation
    • Develop & implement cost savings projects to provide the best total cost solution to the organization
    • Maintain a comprehensive library of reference and historical data
    • Actively work with the business partners to source goods and services in accordance with policies and procedures
    • Ensure the timely execution and delivery of products and services in accordance with business timelines
    • Lead the supplier performance management process for assigned categories
    • Provide strategic insight and access to all relevant spend and related data
    • Ensure that key business stakeholders are engaged, and that procurement strategies fully support the objectives of their business

    Qualifications
    • Bachelor's degree required, MBA (or similar) preferred
    • 5+ years of relevant work experience with strong preference in a large multi-national organization in the biotech/pharmaceutical industry
    • At least 3 years experience in strategic sourcing/category management, conducting cross-functional sourcing projects and negotiating contracts for complex services, with specific experience in Marketing
    • Project background in Agency, Public Relations, Media, Market Research, Medical Education, Conferences, Print, and Direct Marketing highly preferred
    • Strategy development experience 


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  • 11/13/15--00:46: Technical Writer III
  • Requirements :
    - Develop SOP’s for Process assembly and equipment operation - Develop URS’s for new and existing assembly equipment - Develop IQ & OQ equipment process documentation and submit for final approvals - Develop IQ & OQ equipment final reports and submit for final approvals - Help develop final reports from process DOE’s (summarize data reports) - Learn the new documentation system “ Mango “ - Assist all R&D and Engineering in documentation associated with the PDP & TDP product development process - OQ and PQ doc’s will also be required for the equipment and process along with their final reports

     

    Experience:

    10 years experience

    Able to work in a team environment

    Self starter - motivated

     


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  • 11/13/15--01:06: Production Associates
  • For more information, go to: http://www.cwsciences.com/Current-Openings/Production-Associates

     

    Candidates must live local and be a US Citizen or Green Card Holder

    Email resume to: jobs@cwsciences.com

    Commonwealth Sciences is a professional recruiting firm specializing in Science, Engineering and Green Technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors. Our clients value the basic integrity, customer service and industry expertise that defines our organization.

     

    Commonwealth Sciences, Inc.

    www.cwsciences.com


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  • 11/13/15--01:20: Sr. Scientist
  • For more information, go to: http://www.cwsciences.com/Current-Openings/Sr-Scientist

     

    Candidates must live local and be a US Citizen or Green Card Holder

    Email resume to: jobs@cwsciences.com

    Commonwealth Sciences is a professional recruiting firm specializing in Science, Engineering and Green Technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors. Our clients value the basic integrity, customer service and industry expertise that defines our organization.

     

    Commonwealth Sciences, Inc.

    www.cwsciences.com


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    Striving to transform lives through medical science: EMD Serono is the U.S. subsidiary of Merck Serono (parent company Merck KGaA, Darmstadt, Germany). EMD Serono, Inc. is a leader in the U.S. biopharmaceutical industry. We have more than 1,000 employees throughout the United States with fully integrated commercial, clinical, and research operations near Boston.

    EMD Serono has more than 30 trials in our global clinical pipeline, focused on developing innovative therapies for cancer and neurodegenerative diseases such as multiple sclerosis and Parkinson's disease.

    Key Tasks & Responsibility

    • Execute in vitro biochemical assays. 
    • Able to analyze and interpret data and trouble-shoot with supervision.
    • Operates common laboratory equipments as needed.
    • Effectively record and report scientific results
    • Actively interact and closely work with team members Required

    Education:

    • BS degree in biochemistry, biology, or biological science with 1-2 years of experience.
    • Experience in biochemical assay development
    • Proficiency in scientific computer programs including Microsoft Excel and GraphPad Prism
    • Proficient communication skills and record keeping

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    TissueVision is a dynamic, growing company that was founded by MIT researchers. It develops tissue imaging hardware and services for the biomedical imaging market, and its customers include pharmaceutical companies, biotechs, and universities across North America, Europe, and Asia. We are located in an attractive urban area in Somerville, MA and are about a 15 minute walk from Harvard University and 30 minute walk from MIT.

    We are comprised of a mix of biologists, engineers, programmers and scientists, and we are seeking to add to the team a full time mechanical engineer whose job will be to help lead the development of the next version of our tissue imaging and processing platform. In this position, you will be developing instrumentation that directly benefits research in neuroscience, cancer, toxicology, and a host of other application areas.

    This is an excellent opportunity for a talented individual to work in a high visibility role in a smaller company that is on the leading edge of biomedical imaging.

    You will be reporting directly to the CEO and other senior management. Other members of the project include an experienced optomechanical engineer, programmer, and biophysicist. For the younger applicant, this job can grow into a leadership position. For a more experienced applicant seeking a new challenge, this is an excellent opportunity to have more independence than could be found at a large company.

    Responsibilities: Your primary role will be to lead the development of an automated platform for staining and sectioning of tissues and whole organs. Technical skills needed to complete the project will involve a mix of motion control, fluid handling, and automation. Thus, experience with mechatronics, fluidics, automation engineering, CAD, and biological engineering will be helpful. It is a big plus if the person is able to program in some environment, such as Matlab, C, or Python and also knows SolidWorks. Finally, we place an emphasis on candidates that demonstrate the ability to think through a problem rather than a specific set of skills.

    Please include a cover letter and resume with your application.

    Required qualifications

    • PhD plus 2 years of experience, or Bachelor’s degree plus 10 years of experience
    • Mechanical Engineering, Biomedical Engineering, Physics, or related degree
    • Excellent written and verbal communication skills
    • Experience with automation / mechatronics / motion control
    • Attention to detail

    Preferred qualifications

    • Electronics
    • Precision Engineering
    • Matlab / programming experience
    • Prior experience with fluorescence microscopy

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    Primary Duties :
    * Implement medical communication plans in designated disease areas [Neuroscience - ADHD; Neuroscience - Other Indications; GI/IM; Rare Diseases]
    * Manage medical aspects of the global Commercial - Medical - Legal - Regulatory (CMLR) materials review process

    Responsibilities:

    60%: Implement medical communication plans in [Neuroscience - ADHD; Neuroscience - Other Indications; GI/IM; Rare Diseases]
    * Implementation of the medical communication plan for each disease area, including for example, medical materials (print and virtual), event support and disease state education. Coordinate with other members of the [Neuroscience - ADHD; Neuroscience - Other Indications; GI/IM; Rare Diseases] team to identify and implement medical communications best practices
    * Interact with vendor partners supporting Global Medical Communications in the disease area
    * Support implementation of medical communication platform solutions, including, e.g.
    * Medical congress planning and delivery
    * Medical field force tools
    * Digital / multi-channel approaches
    * External materials review and management *

    40%: Manage medical aspects of the global Commercial - Medical - Legal - Regulatory (CMLR) materials review process
    * Conduct day-to-day medical implementation of the Shire CMLR process for promotional materials and review process for non-promotional materials within [Neuroscience - ADHD; Neuroscience - Other Indications; GI/IM; Rare Diseases] . Conduct medical review for one or more disease states / assets
    * Assist other members of the [Neuroscience - ADHD; Neuroscience - Other Indications; GI/IM; Rare Diseases] Global Medical Communication team to ensure CMLR activities are completed efficiently

    Education and Experience Requirements:
    * A relevant healthcare degree is required. A medical or scientific degree (MD, PharmD, PhD, MS or RN) is preferred.
    * >2 years of experience in the biopharmaceutical industry, preferably within a matrix structure
    * >2 years of experience within medical affairs roles (e.g. Medical Science Liaison, Medical Information, Medical Communications, Publications, post doctoral medical communications residency or fellowship)
    * Experience interacting with vendors and managing projects is preferred
    * General knowledge of medical communications approaches and best practices is required
    * Familiarity with regulatory and legal guidelines regarding medical communications strategy and execution

    Other Job Requirements:
    * Availability to travel approximately 20% of time
    * Availability to participate in early or late meetings/teleconferences.

    Shire's Brave culture offers employees with diverse backgrounds the opportunity to enable those with life altering conditions to lead better lives. Shire is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by applicable law. US Applicants who require accommodation in the job application process may contact 484-595-8400.

    Please apply at: Application URL: http://www.aplitrak.com/?adid=amRpZXR6Ljk2Mjk1LjMxNjdAc2hpcmUuYXBsaXRyYWsuY29t


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    Primary Duties :
    * Develop and implement medical communication plans in designated disease areas [Neuroscience - ADHD; Neuroscience - Other Indications; GI/IM; Rare Diseases]
    * Manage medical aspects of the global Commercial - Medical - Legal - Regulatory (MLR) materials review process

    Responsibilities:
    60%:
    Develop and implement medical communication plans in [Neuroscience - ADHD; Neuroscience - Other Indications; GI/IM; Rare Diseases]
    * Collaborate with the Global Medical Team for one or more disease areas / assets to translate medical strategy into medical communication objectives and activities
    * Define and oversee implementation of the medical communication plan for each disease area, including for example, medical materials (print and virtual), event support and disease state education. Coordinate with other members of the [Neuroscience - ADHD; Neuroscience - Other Indications; GI/IM; Rare Diseases] team to identify and implement medical communications best practices
    * Manage vendor partners supporting Global Medical Communications in the disease area
    * Support development and implementation of medical communication platform solutions, including, e.g.
    * Medical congress planning and delivery
    * Medical field force tools
    * Digital / multi-channel approaches
    * External materials review and management

    40%:
    Manage medical aspects of the global Commercial - Medical - Legal - Regulatory (MLR) materials review process
    * Manage and conduct day-to-day medical implementation and optimization of the Shire CMLR process for promotional materials and review process for non-promotional materials within [Neuroscience - ADHD; Neuroscience - Other Indications; GI/IM; Rare Diseases]. Conduct medical review for one or more disease states / assets
    * Collaborate with other members of the [Neuroscience - ADHD; Neuroscience - Other Indications; GI/IM; Rare Diseases] Global Medical Communication team to ensure CMLR activities are allocated and completed efficiently

    Education and Experience Requirements:
    * A relevant healthcare degree is required. A medical or scientific degree (MD, PharmD, PhD, MS or RN) is preferred.
    * >3 years of experience in the biopharmaceutical industry, preferably within a matrix structure
    * >3 years of experience within medical affairs roles (e.g. Medical Science Liaison, Medical Information, Medical Communications, Medical Education, Publications)
    * Experience managing vendors and projects is preferred
    * Good knowledge of medical communications approaches and best practices is required
    * Familiarity with regulatory and legal guidelines regarding medical communications strategy and execution

    Other Job Requirements:
    * Availability to travel approximately 20% of time
    * Availability to participate in early or late meetings/teleconferences.

    Shire's Brave culture offers employees with diverse backgrounds the opportunity to enable those with life altering conditions to lead better lives. Shire is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by applicable law. US Applicants who require accommodation in the job application process may contact 484-595-8400.

    Please apply at: Application URL: http://www.aplitrak.com/?adid=amRpZXR6LjU0MTkxLjMxNjdAc2hpcmUuYXBsaXRyYWsuY29t


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    Org Marketing Statement
    A career at Pfizer offers opportunity, ownership and impact.

    All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere.Our colleagues have the opportunity to grow and develop a career that offers both individual and company success;be part of an ownership culture that values diversity and where all colleagues are energized and engaged;and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry,is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.

    Role Description
    Provide Engineering Tech support related to the qualification of manufacturing processes and equipment within a biopharmaceutical manufacturing facility, such as cleaning validation, cleaning monitoring, cleaning change over, chamber qualification, sterilization qualification.

    Work includes generating validation/qualification documents and execution of qualification activities

    Responsibilities
    * Work with Operations, Quality, Technical groups, and other site/network groups as required to establish business and compliance requirements of the asset.
    * Plan and coordinate the validation work assigned.
    * Technical understanding of process and equipment to be qualified
    * Accountable for quality of work performed.
    * Perform the work in accordance to all of the compliance requirements and in a safe manner.
    * Role will be expected to work Monday - Friday standard shift. Weekends or off hours may be required as needed.

    Qualifications
    EDUCATION AND EXPERIENCE:
    * HS Diploma or GED/Equivalent or prior Military experience required.
    * Hands-on experience is critical in this role of Validation Technician and selected candidates must be able to operate independently and have a minimum of five years working experience in a Biopharmaceutical or pharmaceutical manufacturing facility
    * Candidates must have a solid understanding the Biopharma manufacturing process and operation of the equipment, such as the cleaning processes, SIP processes and autoclaves.
    * Candidate should have an understanding of cGMP systems and practices.
    * Candidate must be able to work across functional areas such as operations, maintenance, quality and regulatory.
    * Good verbal and written communication skills are required.
    * Technical writing and document review skills are required.
    * Understanding of cleaning / steaming processes of the equipment used in the Biopharma manufacturing is preferred.

    PHYSICAL/MENTAL REQUIREMENTS:
    Minimal walking travel as required for meetings and cross functional discussions
    Normal shift: 8AM - 5PM. This may vary according to the business need.

    NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS:
    * Role will be expected to work Monday - Friday standard shift. Weekends or off hours may be required as needed.

    EEO & Employment Eligibility
    Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.

    Please apply at: Application URL: http://www.aplitrak.com/?adid=SmltLlRhdm9saWVyaS44NzU4OS4zMTY3QHBmaXplci5hcGxpdHJhay5jb20


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    Org Marketing Statement
    A career at Pfizer offers opportunity, ownership and impact.

    All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere.Our colleagues have the opportunity to grow and develop a career that offers both individual and company success;be part of an ownership culture that values diversity and where all colleagues are energized and engaged;and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry,is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.

    Role Description
    We are seeking an experienced research scientist to join the CTI-GBT group in our antibody-based therapeutic discovery efforts. The successful candidate will be responsible for lead selection and optimization to develop various immuno-oncology therapeutic modalities employing molecular biology, biochemistry, structural modeling and antibody engineering skills. The candidate is expected to contribute to more than one therapeutic program in parallel, design and execute antibody screening and engineering campaigns employing advanced biochemistry and cell biology techniques and assess therapeutic intervention employing appropriate antibody modalities. The candidate should exhibit excellent collaborative and communication skills working on cross-functional multi-disciplinary teams.

    Responsibilities
    The candidate will be responsible for:
    1. Designing of antibody generation and screening strategy and delivering therapeutic candidates on multiple projects in collaboration with CTI biology teams.
    2. Developing, optimizing and executing high throughout binding assays (ELISA, Octet) for screening antibody panels.
    3. Optimization of antibodies and alternate formats to fit the biology using antibody engineering techniques
    3. Developing cell based assays to characterize hits and leads for binding to Fc receptors and targets expressed on primary cells, assessing effector functions utilizing various sources of effector cells, re-targeting tumor cells to different immune cell types and measuring cytotoxicity.
    4. Documenting experimental data, presenting hypotheses, experimental data, conclusions and interpretations at departmental and cross-functional team meetings.
    5. Contributing to patent application examples, writing scientific publications and presenting at conferences.

    Qualifications
    MS or PhD in molecular/cellular biology, biochemistry, structural biology, immunology or a related discipline with 5-7 years for MS and 2-4 years for PhD of research experience in academia and/or Biotech/Pharmaceutical environment, a record of significant achievements in research, scientific creativity, excellent communication and leadership skills and ability to work in a multidisciplinary, team-oriented environment.
    * Experience in the design, execution, and analysis of biochemical, molecular, and/or cellular assays.
    * Hands-on work experience in the following therapeutic areas: oncology, immunology, inflammatory or autoimmune diseases.
    * Demonstrated experience in cell based assay development to aid the design & testing of therapeutics from discovery to lead-optimization
    * Self-motivated with extremely strong written and oral communication skills, organizational skills, demonstrated ability to work in a highly collaborative environment and ability to achieve high quality results

    Required:
    * Technical proficiency with cell biology pertaining to therapeutic antibody drug discovery and development. Technical skills should include extensive experience with most or all of the following: PCR, RT-PCR, TaqMan, ELISA, immunocytochemistry, advanced FACS analysis and other reliable sophisticated techniques that enable binding and functional assessment of therapeutic antibodies on cells
    * Computational tools for molecular biology and database management, Microsoft Office, GraphPad Prism
    * Experience in structure modeling of antibodies is a plus

    Preferred:
    Prior experience with therapeutic antibody generation and engineering
    Technical expertise in establishment and validation of cell-based assays utilizing primary cells and blood cells especially using FACS, MSD, luminex etc.
    Experience in immunomodulation

    PHYSICAL/MENTAL REQUIREMENTS
    Ability to perform data analysis.

    EEO & Employment Eligibility
    Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.

    Please apply at: Application URL: http://www.aplitrak.com/?adid=QWxpc29uLlR1dGx5cy4yODExNi4zMTY3QHBmaXplci5hcGxpdHJhay5jb20


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    Associate Scientist, T-cell Biologist, at Unum Therapeutics

    Who are we?

    Recent advances in T-cell engineering and antibody therapeutics have led to phenomenal clinical results in oncology, opening the possibility to combine these powerful therapeutic modalities.  Unum Therapeutics was founded with a vision to transform cancer treatment through the discovery, development, and commercialization of novel combination cellular immunotherapies. We’re moving forward fast, are you? Visit www.unumrx.com for our latest news!

    What are we offering to you?

    This is an outstanding opportunity to be a founding member and scientific leader of an early-stage, well funded, start-up company.  You will be a vital part of helping to achieve the Unum vision.  Unum is a place where your input matters and your work will help to drive our company forward.  You will have a direct influence on the science and build the capability of our team.  You will also help to shape the Unum culture and be a part of a passionate, transparent, fast moving and collaborative work environment.  A great place to have impact.

    Where are we?

    Unum is moving to a brand new facility located within walking distance of the Alewife T station. Our new space includes an open layout designed for collaboration and innovation, free parking and conveniently located workout space inside the building.  We are in close proximity to leading academic institutions like MIT and Harvard and to potential pharmaceutical and biotech partners.  This unique location allows for a high level of energy and intellectual exchange within and among fast growing early stage companies.

    What will you be doing?

    • Your main responsibility will be to grow and characterize Primary T-cells

    • Your responsibilities will include assay development and the generation, analysis, and interpretation of key experimental data

    • You will help to build our laboratory efforts by maintaining and creating a productive, fun and exciting environment

    • You will be a valuable contributor to other initiatives as they arise in our fast paced, start-up environment

    Who are we seeking?

    • An independent, flexible, high energy scientist with knowledge of cancer biology and/or immunology

    • MS/BS with 2+ years of experience in cell biology

    • Demonstrated competence with:

      • Primary T-cell and cancer cell line propagation, maintenance, and assay development

      • Characterization of cellular activities – including proliferation, activation, cytokine release, and evaluation of cell killing

      • Flow cytometry

    • Experience with synthetic biology and gene editing techniques, is a plus

    What benefits does Unum offer?

    To attract the very best talent, we are offering an extremely generous package that includes competitive pay, a performance-based bonus, stock options, health and dental insurance coverage, trust-based time off, and commuter/parking benefits.  

    How to Apply?

    Please send cover letter and resume to: careers@unumrx.com

    Unum is an equal opportunity employer.

    We are only accepting applications from candidates with authorization to work in the United States at this time.

    Note to agencies – we are not accepting unsolicited resumes from agencies and will not be responsible for fees associated with any such submittals.


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    Principal Scientist/Director T-cell Biology and Technology, at Unum Therapeutics

    Who are we?

    Recent advances in T-cell engineering and antibody therapeutics have led to phenomenal clinical results in oncology, opening the possibility to combine these powerful therapeutic modalities.  Unum Therapeutics was founded with a vision to transform cancer treatment through the discovery, development, and commercialization of novel combination cellular immunotherapies. We’re moving forward fast, are you? Visit www.unumrx.com for our latest news!

    What are we offering to you?

    This is an outstanding opportunity to be a founding member and scientific leader of an early-stage, well funded, start-up company.  You will be a vital part of helping to achieve the Unum vision.  Unum is a place where your input matters and your work will help to drive our company forward.  You will have a direct influence on the science and build the capability of our team.  You will also help to shape the Unum culture and be a part of a passionate, transparent, fast moving and collaborative work environment.  A great place to have impact.

    Where are we?

    Unum is moving to a brand new facility located within walking distance of the Alewife T station. Our new space includes an open layout designed for collaboration and innovation, free parking and conveniently located workout space inside the building.  We are in close proximity to leading academic institutions like MIT and Harvard and to potential pharmaceutical and biotech partners.  This unique location allows for a high level of energy and intellectual exchange within and among fast growing early stage companies.

    What will you be doing?

    • You will lead the research effort for Unum's therapeutic novel T-cell biology and technology efforts

    • You will be responsible and assure the productivity of a team of scientists.

    • Your team will be responsible for both establishing the core assays by which novel biology and technology are created, and then help transition these to specific pipeline drug candidates. 

    • You will work with our academic medical centers and CROs for the design, analysis, and interpretation of key experimental data.

    • You will mentor, train and direct PhD and non-PhD scientists in these efforts.

    • You will report to the CSO and be a valuable leader and contributor to other initiatives as they arise in our fast paced, start-up environment.

    Who are we seeking?

    • An independent, flexible, high-energy leader and expert in T-cell biology and technology invention, with a demonstrated record of achievements in this area

    • In depth understanding of cancer T-cell biology, with experience building and mentoring discovery scientists

    • PhD with 10+ years of experience in pre-clinical research

    • Demonstrated matrix team leadership and innovative intellectual contributions to

    both pre-clinical and clinical projects

    • Experience with synthetic biology, such as chimeric receptors is a plus

    What benefits does Unum offer?

    To attract the very best talent, we are offering an extremely generous package that includes competitive pay, a performance-based bonus, stock options, health, dental, life and disability insurance coverage, trust-based time off, and commuter/parking benefits.  Relocation assistance is also available to candidates who live outside of the Boston area.

    How to Apply?

    Please send cover letter and resume to: careers@unumrx.com

    Unum is an equal opportunity employer.

    We are only accepting applications from candidates with authorization to work in the United States at this time.

    Note to agencies – we are not accepting unsolicited resumes from agencies and will not be responsible for fees associated with any such submittals.

     


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    Head of Alliance and Project Management, at Unum Therapeutics

    Who are we?

    Recent advances in T-cell engineering and antibody therapeutics have led to phenomenal clinical results in oncology, opening the possibility to combine these powerful therapeutic modalities.  Unum Therapeutics was founded with a vision to transform cancer treatment through the discovery, development, and commercialization of novel combination cellular immunotherapies.  We’re moving forward fast, are you? Visit www.unumrx.com for our latest news!

    What are we offering to you?

    This is an outstanding opportunity to be a founding member and scientific leader of an early-stage, well funded, start-up company.  You will be a vital part of helping to achieve the Unum vision.  Unum is a place where your input matters and your work will help to drive our company forward.  You will have a direct influence on the science and build the capability of our team.  You will also help to shape the Unum culture and be a part of a passionate, transparent, fast moving and collaborative work environment.  A great place to have impact.

    Where are we?

    Unum is moving to a brand new facility located within walking distance of the Alewife T station. Our new space includes an open layout designed for collaboration and innovation, free parking and conveniently located workout space inside the building.  We are in close proximity to leading academic institutions like MIT and Harvard and to potential pharmaceutical and biotech partners.  This unique location allows for a high level of energy and intellectual exchange within and among fast growing early stage companies.

    What will you be doing?

    • You will build and lead the Alliance and Project management teams of the organization across all functions

    • You will develop project plans and associated communications to coordinate, monitor and track all project activities and schedules to ensure quality and timely completion

    • You will prepare and present written and verbal materials to define resource requirements, project workflow, budgets, from internal and external projects

    • You will help lead our teams to generate a vision, establish direction and motivate members, create an atmosphere of trust, leverage diverse views, coach staff, and encourage improvement and innovations

    • You will collaborate with senior/executive leadership in the development and execution of our alliance partner strategy and ensure building successful relationships with external collaborations

    • You will interact with the partners on the various day-to-day needs and drive projects to decisions, attention to detail orientation is critical

    • Ensure good governance including routine reporting to management on alliance activities and results of alliance operations and routine updates to the joint steering committees on financial activities. Ensure tracking and reporting of all alliance activities

    • You will report to the CSO and be a valuable leader and contributor to other initiatives as they arise in our fast paced, start-up environment

    Who are we seeking?

    • PhD or M.Sc. with at least 10+ years of industry leadership experience in alliance and project management

    • Significant experience with both large and small organizations, developing effective partner relationships and building strong working alliances with internal teams and leadership.

    • Proven track record of building and maintaining high performing teams

    • Experience in the biopharmaceutical industry with a detailed understanding of the pharmaceutical industry and the development, manufacturing and commercialization of new drugs, and will have worked in an emerging and commercial stage company.

    • Expertise in current project and alliance management practices and metrics

    What benefits does Unum offer?

    To attract the very best talent, we are offering an extremely generous package that includes competitive pay, a performance-based bonus, stock options, health, dental, life and disability insurance coverage, trust-based time off, and commuter/parking benefits.  Relocation assistance is also available to candidates who live outside of the Boston area.

    How to Apply?

    Please send cover letter and resume to: careers@unumrx.com

    Unum is an equal opportunity employer.

    We are only accepting applications from candidates with authorization to work in the United States at this time.

    Note to agencies – we are not accepting unsolicited resumes from agencies and will not be responsible for fees associated with any such submittals.

     


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