Job Title: Clinical Assays Associate Scientist (Needham, MA)

Summary of Position:

The Associate Scientist will assist in the development and validation of immunoassays, such as ELISA, and conduct analysis of clinical trial patient samples using validated immunoassay methods.

Position Responsibilities:

• For assay development, evaluate biochemical reagents and assist in formatting and optimizing new test methods.
• Characterize assay performance (precision, accuracy, etc.) in validation experiments.
• Analyze biological samples collected from patients participating in clinical trials.
• Manage inventory of patient samples.

Required Skills:

• Basic laboratory skills required to work in a life sciences lab (pipetting, buffer preparation, handling potentially infectious material).
• Basic immunology and understanding of antibody structure & function.
• Basic principles of spectrophotometry, and application in colorimetric assays.
• Familiarity with spreadsheet software (e.g., Excel), and statistical software (e.g., GraphPad Prism)
• Highly organized, able to follow detailed procedures.
• Very interested in learning new concepts and skills, curious about ‘what makes things work’.
• Able to work on multiple projects simultaneously.
• Intent on continual professional growth and development.
• Demonstration of strong communication and organizational skills as well as the ability to work independently as well as in a team.

Education/Experience:

• Bachelor’s degree in biological science, or related discipline.
• Experience with immunoassay methods, for example ELISA, a plus.

Qualified candidates interested in applying for this position at Celldex are invited to submit a resume and cover letter: (please include job title on the subject line)

Human Resources

Celldex Therapeutics, Inc.

119 Fourth Avenue

Needham, MA 02494-2725

E-Mail: hr@celldextherapeutics.com

Summary of Position:

The Document Specialist will be involved in the preparation and review of documents.  This position will work with QA on resolution of deviations, out of specifications, training and general manufacturing compliance.

Position Responsibilities:

• Revise SOPs, batch records and solution records as needed.
• Review executed batch records for completeness and working with QA and the manufacturing group to resolve deviations.
• Collaborate with QA and manufacturing in performing investigations and will be responsible for writing investigative reports.
• Work with QA to ensure manufacturing compliance with GMPs.
• Update logs, databases and catalogues.
• Maintain documentation files. 
• Create status reports.
• Performs other additional job related duties as required.

 Required Skills:

• The ability to write SOPs, deviations, CAPAs, and batch records.
• Strong communication and organizational skills.
• The ability to work independently and as part of a team.

Education/Experience:

• Bachelor’s degree in Biological science, or related discipline or equivalent certificate program. 
• Minimum 2 years experience in Biotech/Pharma industry.
• Minimum 2 years experience in biotechnology cGMP manufacturing.

Qualified candidates interested in applying for this position at Celldex are invited to submit a resume and cover letter: (please include job title on the subject line)

 Human Resources

Celldex Therapeutics, Inc.

119 Fourth Avenue

Needham, MA 02494-2725

E-Mail: hr@celldextherapeutics.com

Don't miss your chance to be considered for a fantastic opening at one of the top biopharmaceutical companies in Massachusetts! If you are a Logistics professional in biotech/pharmaceutical and feel that you're role has become routine, then you need to call me right away.

The role will primarily be split between supporting the commercialization of new products and continuous improvement activities. The role reports into a well respected Manager and will join an accomplished team of Logistics professionals.

The ideal candidate will have experience with GMP guidelines, transportation (import/export), cold chain and pharmaceutical knowledge. They can consider as little as 4-6 years of experience but more experience is also welcome. Although they are Oracle-based, any experience with similar enterprise systems is acceptable.

A formal description can be supplied for interested candidates. Resumes to nuno@hireminds.com to be considered. All resumes will be kept strictly confidential until you choose to pursue a specific opportunity with one of our clients.

Our client is a fast growth global medical device leader. This is a great opportunity if you are seeking to join a highly innovative and financially solid industry leader that promises excellent career growth and challenging leadership opportunities!

Requirements

You will be responsible for the design, installation and management of complex IT infrastructures in LAN and WAN settings. The environment, globally connected, includes a large number of physical and virtual servers, storage area networks (SAN), Wi-Fi devices, Enterprise firewalls, multi-point VPN connectivity, Internet proxies and Ethernet switches.  Additionally, you will be involved in data management, performing systems backup and recovery.  

Essential Qualifications

• Demonstrable analytical and troubleshooting skills
• Ability to communicate technical issues up and down the organization
• 5+ years professional employment designing and deploying IT infrastructure Conversant with all aspects of VMware and vSphere 5.x in a multi-host environment
• SAN storage management using high availability and vMotion
• Experience installing/configuring/administering Storage Area Networks (SAN); EMC preferred
• Cisco Layer 2 and 3 Switch configuration VPN management and support; Cisco AnyConnect preferred Server deployment/administration in a 100+, Windows 2008 environment
• Multi-year experience deploying/administering Linux servers with Red Hat Enterprise or CentOS Conversant in the use and support of Apache, Ruby on Rails, Mongrel and PostgreSQL
• Ability to participate in an after-hours, on-call rotating support schedule
• Bachelor’s Degree in an appropriate discipline from an accredited 4-year college, but non-degreed candidates with multiple IT certifications will be considered

Desirable Qualifications

Backup Exec 2010, EMC Data Domain, EMC Centera Symantec Enterprise Vault AVAYA S8400 telephony, TDM and VOIP Vendor management – LAN/WAN suppliers

Interested candidates should send resumes to Josh Blumenshine at jblumenshine@kingbishop.com

Looking for a candidate to assist the lab manager in supervising a small chemistry group. Responsibilities will include training of technicians, troubleshooting issues that arise and keeping the team on track.

Requirements:

BS/MS Chemistry/Biochemistry with 5 years of lab experience. Supervisory experience is a must.

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

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.

http://www.cwsciences.com

Title: Clinical Research Associate II (USA - Any Region - Home Based)
Department: Clinical Research
Location: USA - Any Region - Home Based
Employment Type: Full Time
Job Type: Regular
Req Number: post-20021140

Company Profile:
PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies.
Given our breadth of expertise and the trust placed in us by major pharmaceutical companies worldwide, PAREXEL can provide you with a number of career options in Clinical Research that can rarely be found within just one company. In fact, over 25% of the positions opened at PAREXEL are filled by current employees working to advance their skills and careers.

Description:
As a Clinical Research Associate (CRA) at PAREXEL, you have the opportunity to be a true clinician and work on complex therapeutic studies. In addition you will act as the on-site resource for the other study team members.

You will have the greatest impact on drug and medical device clinical trials by working on-site with the clients, focusing on the clinical trial, while leveraging the resources of our in-house monitoring team. Because of our unique structure, you will spend less time on the administrative aspects of the trial, and will be able to focus on what you were trained to do. developing close relationships with the sites and having a positive impact on the success of the trial.

Our travel model encourages efficiency so you have more time for meaningful work activities. We are also organizationally and technologically equipped to support your focus on the clinical aspects of your work whether you are on the road or in your office.

We are seeking independent professionals who have the ability to see the big picture and communicate effectively. If you are organized, have strong attention to detail, are able to build lasting relationships with internal and external clients, and demonstrate excellent communication skills. we want you to be the new face at PAREXEL.

Our management is committed to our internal environment of excellence, offering development opportunities and sponsoring initiatives for those employees who bring professional level skill and dedication to their careers. At PAREXEL, you will maximize your ability to reach your personal development and professional career goals.

Experience:
To qualify, you should have at least 1.5 years of on-site clinical monitoring experience.

Please apply via the link below:

http://jobs.parexel.com/home-based/clinical-research-associate/jobid2176937-clinical-research-associate-ii-jobs

Title: Clinical Research Associate II (USA - Any Region - Home Based)
Department: Clinical Research
Location: USA - Any Region - Home Based
Employment Type: Full Time
Job Type: Regular
Req Number: post-20021140

Company Profile:
PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies.
Given our breadth of expertise and the trust placed in us by major pharmaceutical companies worldwide, PAREXEL can provide you with a number of career options in Clinical Research that can rarely be found within just one company. In fact, over 25% of the positions opened at PAREXEL are filled by current employees working to advance their skills and careers.

Description:
As a Clinical Research Associate (CRA) at PAREXEL, you have the opportunity to be a true clinician and work on complex therapeutic studies. In addition you will act as the on-site resource for the other study team members.

You will have the greatest impact on drug and medical device clinical trials by working on-site with the clients, focusing on the clinical trial, while leveraging the resources of our in-house monitoring team. Because of our unique structure, you will spend less time on the administrative aspects of the trial, and will be able to focus on what you were trained to do. developing close relationships with the sites and having a positive impact on the success of the trial.

Our travel model encourages efficiency so you have more time for meaningful work activities. We are also organizationally and technologically equipped to support your focus on the clinical aspects of your work whether you are on the road or in your office.

We are seeking independent professionals who have the ability to see the big picture and communicate effectively. If you are organized, have strong attention to detail, are able to build lasting relationships with internal and external clients, and demonstrate excellent communication skills. we want you to be the new face at PAREXEL.

Our management is committed to our internal environment of excellence, offering development opportunities and sponsoring initiatives for those employees who bring professional level skill and dedication to their careers. At PAREXEL, you will maximize your ability to reach your personal development and professional career goals.

Experience:
To qualify, you should have at least 1.5 years of on-site clinical monitoring experience.

Please apply via the link below:

http://jobs.parexel.com/home-based/clinical-research-associate/jobid2176937-clinical-research-associate-ii-jobs

Title: Clinical Research Associate II (USA - Midwest - Home Base)
Department: Clinical Research
Location: USA - Midwest - Home Based
Employment Type: Full Time
Job Type: Regular
Req Number: post-20021023


Company Profile:
PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies.
Given our breadth of expertise and the trust placed in us by major pharmaceutical companies worldwide, PAREXEL can provide you with a number of career options in Clinical Research that can rarely be found within just one company. In fact, over 25% of the positions opened at PAREXEL are filled by current employees working to advance their skills and careers.

Description:
As a Clinical Research Associate (CRA) at PAREXEL, you have the opportunity to be a true clinician and work on complex therapeutic studies. In addition you will act as the on-site resource for the other study team members.

You will have the greatest impact on drug and medical device clinical trials by working on-site with the clients, focusing on the clinical trial, while leveraging the resources of our in-house monitoring team. Because of our unique structure, you will spend less time on the administrative aspects of the trial, and will be able to focus on what you were trained to do ' developing close relationships with the sites and having a positive impact on the success of the trial.

Our travel model encourages efficiency so you have more time for meaningful work activities. We are also organizationally and technologically equipped to support your focus on the clinical aspects of your work whether you are on the road or in your office.
We are seeking independent professionals who have the ability to see the big picture and communicate effectively. If you are organized, have strong attention to detail, are able to build lasting relationships with internal and external clients, and demonstrate excellent communication skills ' we want you to be the new face at PAREXEL.

Our management is committed to our internal environment of excellence, offering development opportunities and sponsoring initiatives for those employees who bring professional level skill and dedication to their careers. At PAREXEL, you will maximize your ability to reach your personal development and professional career goals.

Experience:
To qualify, you should have at least 1.5 years of on-site clinical monitoring experience.

Please apply via the link below:

http://jobs.parexel.com/home-based/clinical-research-associate/jobid2176924-clinical-research-associate-ii-jobs

Title: Clinical Research Associate II (USA-West-Homebased)
Department: Clinical Research
Location: USA - West - Home Based
Employment Type: Full Time
Job Type: Regular
Req Number: post-00021142

Company Profile:
PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies.
Given our breadth of expertise and the trust placed in us by major pharmaceutical companies worldwide, PAREXEL can provide you with a number of career options in Clinical Research that can rarely be found within just one company. In fact, over 25% of the positions opened at PAREXEL are filled by current employees working to advance their skills and careers.

Description:
Position Summary
As a Clinical Research Associate (CRA) at PAREXEL, you have the opportunity to be a true clinician and work on complex therapeutic studies. In addition you will act as the on-site resource for the other study team members.

You will have the greatest impact on drug and medical device clinical trials by working on-site with the clients, focusing on the clinical trial, while leveraging the resources of our in-house monitoring team. Because of our unique structure, you will spend less time on the administrative aspects of the trial, and will be able to focus on what you were trained to do ' developing close relationships with the sites and having a positive impact on the success of the trial.

Our travel model encourages efficiency so you have more time for meaningful work activities. We are also organizationally and technologically equipped to support your focus on the clinical aspects of your work whether you are on the road or in your office.

We are seeking independent professionals who have the ability to see the big picture and communicate effectively. If you are organized, have strong attention to detail, are able to build lasting relationships with internal and external clients, and demonstrate excellent communication skills ' we want you to be the new face at PAREXEL.

Our management is committed to our internal environment of excellence, offering development opportunities and sponsoring initiatives for those employees who bring professional level skill and dedication to their careers. At PAREXEL, you will maximize your ability to reach your personal development and professional career goals.

Experience:
To qualify, you should have at least 1.5 years of on-site clinical monitoring experience.

Please apply via the link below:

http://jobs.parexel.com/home-based/clinical-research-associate/jobid2176939-clinical-research-associate-ii-jobs

Title: Clinical Research Associate II (USA - Southwest - Home Based)
Department: Clinical Research
Location: USA - Southwest - Home Based
Employment Type:Full Time
Job Type: Regular
Req Number: post-00022147


Company Profile:
PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies.

Given our breadth of expertise and the trust placed in us by major pharmaceutical companies worldwide, PAREXEL can provide you with a number of career options in Clinical Research that can rarely be found within just one company. In fact, over 25% of the positions opened at PAREXEL are filled by current employees working to advance their skills and careers.

Description:
As a Clinical Research Associate (CRA) at PAREXEL, you have the opportunity to be a true clinician and work on complex therapeutic studies. In addition you will act as the on-site resource for the other study team members.

You will have the greatest impact on drug and medical device clinical trials by working on-site with the clients, focusing on the clinical trial, while leveraging the resources of our in-house monitoring team. Because of our unique structure, you will spend less time on the administrative aspects of the trial, and will be able to focus on what you were trained to do ' developing close relationships with the sites and having a positive impact on the success of the trial.

Our travel model encourages efficiency so you have more time for meaningful work activities. We are also organizationally and technologically equipped to support your focus on the clinical aspects of your work whether you are on the road or in your office.

We are seeking independent professionals who have the ability to see the big picture and communicate effectively. If you are organized, have strong attention to detail, are able to build lasting relationships with internal and external clients, and demonstrate excellent communication skills ' we want you to be the new face at PAREXEL.

Our management is committed to our internal environment of excellence, offering development opportunities and sponsoring initiatives for those employees who bring professional level skill and dedication to their careers. At PAREXEL, you will maximize your ability to reach your personal development and professional career goals.

Experience:
To qualify, you should have at least 1.5 years of on-site clinical monitoring experience.

Please apply via the link below:

http://jobs.parexel.com/home-based/clinical-research/jobid3193280-clinical-research-associate-ii-jobs

Title: Clinical Research Associate II (USA - Upper Central - Home Based)
Department: Clinical Research
Location: USA - Upper Central - Home Based
Employment Type: Full Time
Job Type: Regular
Req Number: post-20021026

Company Profile:
PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies.

Given our breadth of expertise and the trust placed in us by major pharmaceutical companies worldwide, PAREXEL can provide you with a number of career options in Clinical Research that can rarely be found within just one company. In fact, over 25% of the positions opened at PAREXEL are filled by current employees working to advance their skills and careers.

Description:
As a Clinical Research Associate (CRA) at PAREXEL, you have the opportunity to be a true clinician and work on complex therapeutic studies. In addition you will act as the on-site resource for the other study team members.

You will have the greatest impact on drug and medical device clinical trials by working on-site with the clients, focusing on the clinical trial, while leveraging the resources of our in-house monitoring team. Because of our unique structure, you will spend less time on the administrative aspects of the trial, and will be able to focus on what you were trained to do ' developing close relationships with the sites and having a positive impact on the success of the trial.

Our travel model encourages efficiency so you have more time for meaningful work activities. We are also organizationally and technologically equipped to support your focus on the clinical aspects of your work whether you are on the road or in your office.

We are seeking independent professionals who have the ability to see the big picture and communicate effectively. If you are organized, have strong attention to detail, are able to build lasting relationships with internal and external clients, and demonstrate excellent communication skills ' we want you to be the new face at PAREXEL.

Our management is committed to our internal environment of excellence, offering development opportunities and sponsoring initiatives for those employees who bring professional level skill and dedication to their careers. At PAREXEL, you will maximize your ability to reach your personal development and professional career goals.

*LI-EC1

Experience:

To qualify, you should have at least 1.5 years of on-site clinical monitoring experience.

Please apply via the link below:

http://jobs.parexel.com/home-based/clinical-research/jobid2176936-clinical-research-associate-ii-jobs

Looking for a candidate to assist the lab manager in supervising a small chemistry group. Responsibilities will include training of technicians, troubleshooting issues that arise and keeping the team on track.

Requirements:

BS/MS Chemistry/Biochemistry with 5 years of lab experience Supervisory experience is a must

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

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.

http://www.cwsciences.com

Duties:

Negotiate and finalize clinical trial agreements, contract research organizations (CROs) agreements, general service agreements, consultancy agreements, and lab services. Identifies potential vendors and negotiates budgets. Collaborates with clinical trial team, study start up groups, Investigational sites and vendors to verify and develop budget and negotiated cost savings. Works closely with clinical trial team and study start up teams to ensure delivery of fully executed contracts in support of timely study start-up to meet departmental and organizational goals.

Requirements:

• BS/MS with at least 5 years experience at a pharmaceutical company or CRO
• Minimum of 3 years experience in contract negotiation and preparation and familiarity with legal terminology associated with the pharmaceutical industry.
• Experience with the negotiation of contract terms, pricing, payment schedules, Confidentiality Agreements (CDAs), generation of the final contract, and management of ongoing vendor collaborations     

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

Duties:

Act as the primary support engineer for instrumentation by keeping instruments running at their optimum performance through proactive preventive maintenance. Monitor performance of equipment by implementing QC standard operating procedures

Requirements:

• AS/BS in Life Sciences with 1-5 years' experience in an industry setting
• Ability to diagnose and remedy advanced hardware and software problems quickly.
• Experience with HPLC (Prep and/or Analytical) techniques, instrumentation and underlying principles
• Basic laboratory skills including preparing solvents, standards, and solutions preps
• Strong PC skills in Windows 7 or XP OS
• Working knowledge of MS Office     

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

Participate in study specific meetings, assist with cost tracking, assemble all necessary documentation for clinical trials, assist with regulatory and ethical regulations, and assemble/maintenance and archiving of the TMF.

Requirements:

BS/MS in Biology or related field with 1+ years experience in a clinical setting. Must have experience assembling, maintaining, and archiving TMFs Must have experience with budget reconciliation

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

Position Description:

Candidate in this position be involved in research and development activities using scientific and mathematical techniques to develop and analyze data. Will conduct a variety of experiments to evaluate the use and efficacy of ELISA based products. Duties will include handling blood and antibody samples, documenting and reporting results.

Requirements:

Candidate must have a B.S. or M.S. in a related life science with 2-5 years of post-curriculum experience developing ELISA’s & bioassays. Must have excellent oral and written communication skills as well as strong computer & spreadsheet skills.

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

Position Description:

The Quality Assurance Specialist will implement and coordinate assurance programs to improve the quality of new and existing products. Responsibilities include participating in Quality System Management meetings, coordination between departments, reviewing QA problems, maintenance of change controls, validations, SOP’s, batch records, etc.  

Requirements:

Candidate must have a BS or MS degree with 2-5 years of industry experience in quality systems within a GMP environment.  Must be detail oriented with excellent written and oral communication skills.

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

Candidate will join a DMPK group and be responsible for the development and optimization of LC/MS methods for biological sample analysis.   Will also perform data analysis and interpretation.

Requirements:

BS/MS in Biochemistry or related field with 3+ years experience developing and optimizing LC/MS methods in a DMPK environment.

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

Our client is looking for a talented and highly motivated scientist to join a  biochemistry group.  The successful candidate will analyze samples using LC/MS  and perform routine maintenance on the instrument.

Responsibilities:

Operation of LC/MS for sample analysis Perform data analysis and  interpretation

Requirements:

BS/MS in Biochemistry or related field with 1+ years experience running an  LC/MS

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

Candidate assures that samples arriving in the lab are tracked and triaged appropriately and is the key liaison between Biomarker Trial Heads, individual clinical sites submitting material, and analysis vendors.

Requirements:

• Assisting pathologists in data uploads and responding to queries from data management • Maintenance of lab databases • Logging in of specimens and following up with CROs and clinical sites when data is missing • Distribution of samples to vendors, internal labs for analysis • BS in life sciences - Formal qualification as a medical laboratory technician or histotechnician is

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