Principal Researcher, DMPK 9/16/2016

Eisai Andover, MA

Company
Eisai
Job Classification
Full Time
Company Ref #
3839BR
AJE Ref #
576196543
Location
Andover, MA
Experience
Mid-Career (2 - 15 years)
Job Type
Regular
Education
Bachelors Degree

JOB DESCRIPTION

APPLY
Department Name
DMPK US

Location/Territory Name
Andover, MA

Job Description
Responsible for bioanalysis of drug development and clinical projects. The primary role of the Principal Researcher is to develop and validate LC-MS/MS methods, perform sample analysis, and data tabulation for pharmacokinetic (PK) and toxicokinetic (TK) studies. The duties also include preparation of method validation protocols and study reports, presentation of analytical and PK/TK results to project teams, and compiling analytical reports for regulatory submissions. The results generated may have direct or indirect impact on projects advancement/discontinuation.

Responsibilities include but are not limited to:

- Operate LC-MS/MS instruments efficiently and conduct routine troubleshooting independently
- Develop and validate LC-MS/MS and/or ELISA methods for new chemical and biological entities
- Develop scientifically-sound assays independently, based on existing or literature procedures
- Analyze samples for pharmacokinetics and toxicokinetics to support milestone achievement of projects at various stages of drug development
- Maintain laboratory equipment, and train others in its use.
- Communicate effectively with project teams to ensure reliable and efficient delivery of analytical and PK results. Participate in research group discussion and project meetings.
- Communicate research results to supervisor in a timely manner
- Utilize literature searches to solve specific research and assay development issues independently

Job Qualifications
B.S. (5-7 years experience) or M.S. (3-5 years experience) in Analytical Chemistry/Biology, Pharmaceutical Sciences.
Excellent analytical skills, specifically in LC-MS/MS and/or ELISA.
Familiar with regulatory requirement for method validation.
Good knowledge in pharmacokinetics concepts.
Experience in software for lab information management and pharmacokinetic analysis, such as Watson and WinNonlin.
Good time management skills and capable of independently design efficient and well-controlled experiments.
Good communication and presentation skills
Limited Travel: Less than 5% to attend meetings and conferences, etc.

Auto req ID
3839BR

Job Type
Full-time



Eisai is an Equal Opportunity Employer Minority / Female / Disability / Vet