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clinical research in San Francisco Bay Area

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  1. REG AFFAIRS PROJ MGR - (14000005T6) (RK) A

    REG AFFAIRS PROJ MGR - (14000005T6) (RK) A Pharmaceutical / Biotech  Legal - Regulatory / Compliance Law Full-time United States - California - Santa Clara Jobs ID - 1040501 The Compensation Benefits - Full Bonus Eligible - Yes Interview Travel Reimbursed - Yes Detailed Job Description Job Description REG AFFAIRS PROJ MGR(Job Number: 14000005T6) Primary Job Function  As an individual contributor, the function of a Regulatory Affairs Project Manager is to combine knowledge of scientific, ...

  2. Clinical Document Associate

      Our client has a permanent Clinical Document Specialist position available in Mountain View, CA. Purpose of Position To support ongoing essential document collection and handling from multiple, global clinical studies.  Summary: The ideal candidate should be comfortable working within a dynamic, fast paced environment including communicating with different functional areas CSMs, contractors, and vendors, as requested.  Would also be eager to take on new responsibilities and support the team in ...

  3. Senior Associate, Outsourced Manufacturing-Pharma

    Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. Our worldwide staff of more than 5,000 people is a close community where you can see the tangible results of your contributions, where every individual matters, and ...

  4. 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, ...

  5. $5K Sign On Bonus- CRA  Monitors Needed - Set Yourself Up for Success

    CRAs - Join Covance and receive a $5000 Sign On Bonus! Meet the CRA hiring team at the ACRP conference - email [email removed].   Set yourself up for SUCCESS with Early Clinical Development! Now is the time to join our growing business where you have supportive management and a cohesive team. At Covance, you are not just a number. We value you and your hard work...we want you to succeed.   URGENT Need for Oncology Monitors! Calling all Experienced Clinical Research Associates / CRAs / Monitors ...

  6. (Sr) Clinical Trial Manager – Contract or Full Time (SF Bay Area)

    DESCRIPTION: Independently lead clinical trial project execution to ensure that trial timelines, costs, and quality metrics are met for a Phase 1 oncology trial Serves as primary contact for functional area representatives in managing the financial aspect of clinical trials to ensure accuracy and timeliness of service provider and site payments. Oversight for forecasting of clinical supplies Manage study milestones to ensure accurate tracking and reporting of study metrics. Manage trial ...

  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. Principal Scientist

     Job Id # 54156                                                               Principal Scientist   Location: Pleasanton, CA   Description: This position is hybrid position that will focus more on Business of Diagnostics and Technical Diagnostics from a clinical research perspective. There will be an emphasis on Clinical Trials however will not be a position that will take place inside the labortory setting.  Someone who has a strong background working in a laboratory is preferred to have full ...

  9. 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 ...

  10. 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 ...

  11. 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 ...

  12. 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!

  13. 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, ...

  14. 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 ...

  15. 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 ...

  16. 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 ...

  17. 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 ...

  18. 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 ...

  19. Clinical Data Coordinator

    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 ...

  20. 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 ...

  21. 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 ...

  22. 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 ...

  23. 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 ...

  24. 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, ...