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biotechnology in San Francisco Bay Area

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  1. Scientist Research and Development

    Job Id # 54185 Scientist  Research & Development Location: Pleasanton, CA Length: 6 Months Description: Responsibilities: includes but not limited to the following: • Plan, execute and document research experiments, analyze and present data • Perform nucleic acid extraction, and quantification from Whole blood, Plasma, buccal cells or other clinical samples. • Formulate simple and complex reagents, monitors laboratory supplies, and assures proper use and maintenance of lab equipment.  • Design ...

  2. Scientist, Translational Development

    Our client, a large reputable pharmaceutical company, is currently seeking a Scientist, Translational Development. Under moderate supervision in a fast-moving team-based environment, the Contractor will provide biomarker specimen and clinical trial support across multiple studies in oncology and inflammation/immunology, execute on biospecimen operations logistics, track biospecimens using a laboratory inventory management system, and provide biospecimen processing training. As part of the ...

  3. Senior Clinical Research Associate(office based) - Contract

    Our client, a growing biotechnology company in the San Francisco, CA area is looking for a contract  Senior CRA to work office based in their San Rafael offices(this is not a home based opportunity). The Senior CRA will provide oversight work (vendor management, site management, data review, trip report reviews, etc.).  PKU experience required. Metabolic experience a plus!

  4. Regulatory Affairs Associate

    Harvest Technical is seeking an Associate, Regulatory Affairs  for our Biotech client in the Greater Bay Area. Description:        The Associate, Regulatory Affairs is responsible for the coordination, preparation and submission of a variety of regulatory submissions including INDs, CTAs, BLAs and NDAs to regulatory authorities. RESPONSIBILITIES Attend project team meetings across functional areas Prepare, submit, and maintain domestic and international regulatory filings, both ...

  5. Associate Director of Biostatistics

    Associate Director of Biostatistics – San Francisco The position will standardize Biostatistics processes to gain efficiencies in both external outsourcing and internal quality.  It will also require extensive interaction with internal and external stakeholders directly contributing to and /or overseeing clinical study planning and analyses. • Provide statistical expertise to new drug development programs as a Subject Matter Expert in Biostatistics and provides statistical leadership in the design ...

  6. Scientist II-3986763

    Job Duties Responsibilities: includes but not limited to the following: Plan, execute and document research experiments, analyze and present data Perform nucleic acid extraction, and quantification from Whole blood, Plasma, buccal cells or other clinical samples. Formulate simple and complex reagents, monitors laboratory supplies, and assures proper use and maintenance of lab equipment. Design and evaluate real-time PCR primers/ TAQMAN probes; optimize PCR amplification parameters for SNP ...

  7. Validation Engineer - West Region

    ProPharma Group is an industry leader providing validation, compliance and technical services to the pharmaceutical, biotechnology, medical device and related industries. We offer the excitement of a consistently evolving career. Our team is continually learning and working on new and exciting projects in a variety of regions. We look for people who excel in their technical area of expertise, believe in our values of Experience, Integrity and Commitment and thrive in the collaborative, rigorous and ...

  8. CLINICAL RESEARCH ASSOCIATE / TRIAL MONITOR (Training & Jobs)

     CLINICAL RESEARCH ASSOCIATE / TRIAL MONITOR   COMPANY: QTECH SOLUTIONS INC., (Since 2000) Like US : https://www.facebook.com/QtechSolutionsInc Helping students and professionals since 2000, please call us or email your resume for Job assistance.   Qtech Solutions Inc. (Qtech-Sol), DBA Qtech-Sol Professional Development Center (QPDC) with locations in NJ (Headquarters), CA (Regional) and India (Offshore), is a Software Development & Training Organization.   Qtech's Training Division is a ...

  9. DRUG SAFETY / PATIENT SAFETY DATA SPECIALIST (Training & Jobs)

    DRUG SAFETY ASSOCIATE / PATIENT SAFETY SPECIALIST   COMPANY: QTECH SOLUTIONS INC., (Since 2000) Like US : https://www.facebook.com/QtechSolutionsInc Helping students and professionals since 2000, please call us or email your resume for Job assistance.   Qtech Solutions Inc. (Qtech-Sol), DBA Qtech-Sol Professional Development Center (QPDC) with locations in NJ (Headquarters), CA (Regional) and India (Offshore), is a Software Development & Training Organization.   Qtech's Training Division is a ...

  10. Clinical Data Managers (Oncology)

    Partner with Inventiv Health to support the Oncology trials of this Bay Area Biotechnology company. Education: • BS/BA degree in related discipline and 6 years of related experience; or, • Equivalent combination of education and experience. Experience: • Experience in Biotech/Pharmaceutical industry preferred. • A minimum of 5 years of clinical data management experience is also required, some of which is preferred to have been in the pharmaceutical industry or clinical trials. • Experience with ...

  11. ~~Regional Clinical Research Associates needed (West Coast)

    Job Description A highly reputable & distinguished corporation is currently looking for Regional Clinical Research Associates needed (location) Job Description • Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (60% travel with 75% at peak times) for GCP compliance according to company SOPs and/or client guidelines • Recruit investigators for participation in clinical trials • Negotiate study budgets with investigators • Obtain, review for appropriateness, and ...

  12. Associate (Histologist/Pathologist) (S2393L)

    Our client is a world leading human therapeutics company in the biotechnology industry. We are seeking an Associate to assist the Pathology Department for approximately 5 months with a possible extension. Job Summary: The position will be in the Pathology Department to help support the basic histology and tissue staining. Responsibilities include gross trimming, processing, embedding, sectioning, staining, screening, and imaging tissue samples from research projects. Assay development of new special ...

  13. Principal Consultant - CSV

    ProPharma Group is an industry leader providing validation, compliance and technical services to the pharmaceutical, biotechnology, medical device and related industries. We offer the excitement of a consistently evolving career. Our team is continually learning and working on new and exciting projects in a variety of regions. ProPharma Group develops long-term relationships with clients across the country to which we provide a wide array of value-added services that complement and support their core ...

  14. 3950283 - Scientist II

    Responsibilities: Plan, execute and document research experiments, analyze and present data. Perform RNA extraction, and quantification from formalin fixed paraffin embedded tissue (FFPET), core needle biopsy, plasma, and other clinical samples. Formulate simple and complex reagents, monitors laboratory supplies, and assures proper use and maintenance of lab equipment. Design and evaluate real-time PCR primers/probes; optimize PCR amplification parameters for CoDx Biomarker assay development. ...

  15. 3949796 - Analytical Scientist

    Responsibilities:   Perform routine sample testing and analysis in a fast paced lab for in process, release, stability, and non-routine samples. Observe established turnaround times including timely data review and trending. Execute method transfer of new analytical procedures. Maintaining up to date records of all Analytical study activities in their laboratory notebooks according to cGMP and corporate documentation requirements Ensuring the Analytical laboratory is stocked at all times with ...