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drug safety in San Francisco Bay Area

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  1. Clinical Trial Mgr / CTM III / Full Time / SF Bay Area

    Our San Francisco Bay Area client has asked us to locate, qualify and present a Clinical Trial Manager with 5 years of experience (2 yrs oncology).  Candidate will be responsible for and/or assisting with the execution of Investigator-Sponsored Trials and Client-sponsored hematological clinical trials from protocol concept through clinical study report. Primary Responsibilities and Duties:•Coordinate with investigators and investigator sites . •Coordinate and/or participate in investigator meetings ...

  2. Contract Drug Safety Associate - 6-12 m - Multiple openings

    Title of Position: Contract Drug Safety Specialist Location (Full work location address): South San Francisco, CA Contract Length:  6 -12 months extendable   Provides Drug Safety expertise in insuring the quality documentation of safety data, particularly serious adverse events (SAEs) and for supporting all major tasks related to the management and best utilization of the Argus Safety Database. Ensures compliance with FDA/International Drug Safety regulations in all aspects of drug safety data ...

  3. Clinical Scientist

      SUMMARY: •Perform data review of prepared subject narratives • Perform activities related to interim analysis and data base lock e.g. data cleaning clinical data review • Analyze and interpret study data and support preparation of reports for the FDA. Proactively provide feedback on emerging clinical and competitive trends. Education: • BSN, MS,MSN, Pharm.D., PhD or M.D. in related discipline and five or more years of related experience, or; • Equivalent combination of education and experience. ...

  4. QC Analyst

    QC Analyst (Contract position) Conduct specific biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) and medical devices through all stages of the manufacturing process from incoming raw materials to finished goods, and may include environmental monitoring programs.   Essential Duties and Responsibilities: • Perform environmental monitoring of ISO 5, 7, 8, and 9 cleanrooms at the manufacturing facilities. • Use a variety of laboratory instrumentation and ...

  5. Director Drug Safety Science (perm)

    Looking for strong Safety Surveillance experience, must have management experience as this position will manage other staff.   Minimum REQUIREMENTS: Pharm.D., Ph.D. or M.D. Minimum of 7-10 years experience with pharmacovigilance or clinical drug safety including risk/benefit analysis and safety assessment Excellent clinical judgment and ability to communicate complex clinical issues in a scientifically sound and understandable way Must have excellent writing and communication skills ...

  6. Clinical Trial Mgr / CTM III / Full Time / SF Bay Area

    Our San Francisco Bay Area client has asked us to locate, qualify and present a Clinical Trial Manager with 5 years of experience (2 yrs oncology).  Candidate will be responsible for and/or assisting with the execution of Investigator-Sponsored Trials and Client-sponsored hematological clinical trials from protocol concept through clinical study report. Primary Responsibilities and Duties:•Coordinate with investigators and investigator sites . •Coordinate and/or participate in investigator meetings ...

  7. Clinical Trial Mgr / CTM III / Full Time / SF Bay Area

    Our San Francisco Bay Area client has asked us to locate, qualify and present a Clinical Trial Manager with 5 years of experience (2 yrs oncology).  Candidate will be responsible for and/or assisting with the execution of Investigator-Sponsored Trials and Client-sponsored hematological clinical trials from protocol concept through clinical study report. Primary Responsibilities and Duties:•Coordinate with investigators and investigator sites . •Coordinate and/or participate in investigator meetings ...

  8. 3883424 - BioSpecimen Management Scientist I (II), Panel Production

      Opportunity to participate on a team dedicated to the planning, design, implementation, and execution of panel production project plans within BioSpecimen Management service group.   Ideal candidate has experience in molecular biology laboratory techniques, understands and/or has experience in Good Manufacturing Practices – and is customer-service oriented.  The ability to work independently and manages own work flow to accomplish assigned objectives is a must.   Specific duties will include: ...

  9. Clinical Trial Mgr / CTM III / Full Time / SF Bay Area

    Our San Francisco Bay Area client has asked us to locate, qualify and present a Clinical Trial Manager with 5 years of experience (2 yrs oncology).  Candidate will be responsible for and/or assisting with the execution of Investigator-Sponsored Trials and Client-sponsored hematological clinical trials from protocol concept through clinical study report. Primary Responsibilities and Duties:•Coordinate with investigators and investigator sites . •Coordinate and/or participate in investigator meetings ...

  10. Clinical Trial Mgr / CTM III / Full Time / SF Bay Area

    Our San Francisco Bay Area client has asked us to locate, qualify and present a Clinical Trial Manager with 5 years of experience (2 yrs oncology).  Candidate will be responsible for and/or assisting with the execution of Investigator-Sponsored Trials and Client-sponsored hematological clinical trials from protocol concept through clinical study report. Primary Responsibilities and Duties:•Coordinate with investigators and investigator sites . •Coordinate and/or participate in investigator meetings ...