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clinical research in San Francisco Bay Area

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  1. Medical Advisor (Nationwide)

    Our client is seeking a Medical Advisor II that will provide medical and scientific support to both internal team members and external healthcare decision makers and respond to information inquiries. The Medical Advisor will provide scientific support to the commercial activities, research, marketing, and report safety issues within the region consistent with legal and regulatory requirements.   Responsibilities: •Develop and manage relationship with Thought Leaders through scientific exchange ...

  2. 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!

  3. Associate Director, Clinical Data Management / CDM / SF Peninsula

    CLIENT IS REQUESTING 5+ YRS OF CURRENT ONCOLOGY EXPERIENCE ~~The Associate Director of CDM manages and mentors the CDM staff and leads the effort to develop and maintain all standard operating procedures and business practice guidelines related to CDM and to implement the CDASH standards; leads business activities within the CDM group of Biometrics and the CDM standardization processes; oversees the day to day CDM support of CLIENT’s clinical studies; closely works with the head of Biometrics, ...

  4. PT Study Manager-under the title  Research Analyst (TMF, CSR)

      Study Manager/Associate Study Manager - PART-TIME (20+HRS) Educational Requirements:Bachelor’s degree or equivalent is required • Must have3+ years of direct clinical research experience • Study management experience preferred. Special Skills Needed: • Learns, fast, grasps the 'essence' and can change the course quickly where indicated. • Experience with audit / inspection readiness at site and CRO level preferred • Responsible for compliance with applicable policies and procedures. • Detail ...

  5. Clinical Trial Assistant - (Permanent)

    A highly reputable & distinguished pharmaceutical corporation is currently looking for a qualified and interested Clinical Trial Assistant to work in Sunnyvale, CA. Description Support Clinical Operations to ensure studies are completed, on time, within budget and in compliance with SOPs, FDA regulations and ICH/GCP guidelines. Key Accountabilities/Core Job Responsibilities: Set up CTMS system, as appropriate Assist in preparation of documents including regulatory document templates, study ...

  6. Clinical Data Manager

      A Clinical Data Manager is needed in South San Francisco, CA Job Description:   SUMMARY: Designs, implements and maintains clinical trial database for new and ongoing clinical research studies. Manages clinical database activities including: archiving of clinical data and clinical study databases, security administration, electronic data received from clinical trial sites and vendors, and the development of technical study documents such as annotated case report forms.   ESSENTIAL DUTIES AND ...

  7. Sr Java Developer (Technical Lead)

    Software Engineering at Veracyte It’s an exciting and unique time to join the Veracyte Software & Development Team. Based on our company’s outstanding success with our first commercial solution along with our rich product pipeline, we are doubling the engineering team to meet the demand for IT solutions. We have career opportunities for java software developers, software testers, and business intelligence professionals. This team of engineering professionals will make an immediate impact by ...

  8. 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 ...

  9. Clinical Data Manager

     Title of Position: Temp Clinical Data Manager Location South San Francisco, CA Zip Code:94080 # of position openings:  1 Contract Length:  ---6 -12 months extendable   SUMMARY: Designs, implements and maintains clinical trial database for new and ongoing clinical research studies. Manages clinical database activities including: archiving of clinical data and clinical study databases, security administration, electronic data received from clinical trial sites and vendors, and the development of ...

  10. Senior Medical Science Liaison - MSL

    MUST LIVE IN CALIFORNIA OR NEVADA   We currently have an opening for Medical Science Liaison in the West Coast(territory: California, Nevada, Utah, Oregon, Washington & Hawaii). The Medical Science Liaison will function as a medical and scientific expert in Dermatology, and interact with healthcare decision makers to communicate and advance the scientific platform in alignment with goals and objectives. Responsible for engaging with Key Opinion Leaders, HCPs, institutions and other organizations ...

  11. Senior Medical Science Liaison - MSL

    MUST LIVE IN CALIFORNIA OR NEVADA   We currently have an opening for Medical Science Liaison in the West Coast(territory: California, Nevada, Utah, Oregon, Washington & Hawaii). The Medical Science Liaison will function as a medical and scientific expert in Dermatology, and interact with healthcare decision makers to communicate and advance the scientific platform in alignment with goals and objectives. Responsible for engaging with Key Opinion Leaders, HCPs, institutions and other organizations ...

  12. Director of Regulatory Affairs

    The Director of Regulatory will develop strategies for worldwide regulatory approval and introduction of the current generation and future generations of this clients medical device to market. Responsibilities: This position is responsible for, but not limited to, the following: Develop a sense of regulatory leadership in the division on how the company will have a top notch regulatory system for the division’s development efforts. Work with the clinical team to achieve regulatory approvals for ...

  13. Research Associate 1 – 6 Month Contract (San Jose Area)

      DESCRIPTION:   Responsible for execution of in vitro and in vivo experiments, including tissue culture, apoptosis assays, biological assays, western blotting, molecular biology and animal tumor models and generally supporting preclinical project teams in screening new compounds in cellular assays. Tissue culture biological assays, molecular biology, western blotting, spectrophotometry and microscopy. Small animal tumor models.  Development/execution of in vitro and ex vivo cell based assays ...

  14. Associate Director, Clinical Data Management / CDM / SF Peninsula

    CLIENT IS REQUESTING 5+ YRS OF CURRENT ONCOLOGY EXPERIENCE ~~The Associate Director of CDM manages and mentors the CDM staff and leads the effort to develop and maintain all standard operating procedures and business practice guidelines related to CDM and to implement the CDASH standards; leads business activities within the CDM group of Biometrics and the CDM standardization processes; oversees the day to day CDM support of CLIENT’s clinical studies; closely works with the head of Biometrics, ...

  15. 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 ...

  16. Product Development Manager

    The Product Development Manager will support activities with expertise in drug formulation, product manufacturing and regulatory. The Product Development Manager will provide support in managing contractors. This role provides formulation expertise and selects the most appropriate formulation for pre-clinical, clinical and commercial use. The incumbent solves problems related to formulation, supply or other drug product or drug substance challenges, leads in the outsourcing effort toward the ...

  17. Sr. Core Team Leader - Process / Six Sigma

    As the business leader of a multi-functional (and cross-regional) team within a matrix organization, the Sr. Core Team Leader (CTL) is responsible for ensuring the timely development and successful commercialization of one or more complex BD Biosciences product programs. The Sr. CTL leads the cross functional team through the process from conceptualization, to commercialization. The Sr. CTL blends knowledge of the global market environment with the varying needs BD customers across all geographies. ...

  18. Research Associate II

    Leading pharma client seeksa Research Associate for a 3 month contract. Summary: - Performs research and / or product development in collaborationwith others to develop drug products (inhalation powder and inhaler) fromtoxicology studies to clinical phases of development. - Characterizes physicochemical and aerosol performance offormulations and drug products. - Exercises technical judgment in the execution and interpretationof experiments. - Contributes to project progress within a scientific ...

  19. 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 ...

  20. CLINICAL SAS PROGRAMMER / DATA MANAGEMENT (Training & Jobs)

      CLINICAL SAS PROGRAMMER / DATA MANAGEMENT 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 ...

  21. 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 ...

  22. Associate Director, Clinical Data Management / CDM / SF Peninsula

    CLIENT IS REQUESTING 5+ YRS OF CURRENT ONCOLOGY EXPERIENCE ~~The Associate Director of CDM manages and mentors the CDM staff and leads the effort to develop and maintain all standard operating procedures and business practice guidelines related to CDM and to implement the CDASH standards; leads business activities within the CDM group of Biometrics and the CDM standardization processes; oversees the day to day CDM support of CLIENT’s clinical studies; closely works with the head of Biometrics, ...

  23. Research Associate

    My name is Starr and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Research Associate for a prominent client of ours.  This position is located in San Carlos, CA. Details for the positions are as follows:   Job Description:   Function A majority of the testing will be stability and clinical "lot release" - some of the testing will be Raw Material Testing Responsible for generation, review and approval of LIMS results Ensure that all activities are ...

  24. ~~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 ...