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clinical research in Orange County

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    1. Life Cycle Management - Clinical Marketing

      Life Cycle Management/Clinical Marketing Kelly Scientific has an opening in Irvine, CA for a Life Cycle Manager. Job Duties: Reports to the Senior Manager, Franchise Life Cycle Management of Medical Operations for the therapeutic space Franchise Life Cycle Management Support ...

    2. Medical Affairs Specialist

      Medical Affairs Specialist - Life Cycle Management Medical OperationsKelly Clinical Research has an immediate opening for a Medical Affairs Specialist supporting a global developer of innovative infection prevention solutions and educational programs. The position is based ...

    3. Clinical Project Manager

      Summary:   WCCT Global has a unique process-based management approach, which helps to establish a clear vision of a project and to define the strategy, structure, and resources required to achieve success. From the start to completion of a clinical research study, the ...

    4. Clinical Research Associate II

      POSITION SUMMARY: Assist in preparation of clinical protocols and FDA submissions. Perform site initiation and close-out visit, reviews and audit data collection forms, participate in Investigator Meetings, assist in physician training, train site research coordinators, ...

    5. Insurance Collector

       Ambry Genetics Corporation is a genetic testing laboratory that provides clinical diagnostics testing services for genetic conditions. We have a highly adaptable, ever changing work environment. You’ll notice right away our employees are passionate about their work and the ...

    6. Lab Assistant

      Enter Summary:   The Lab Assistant I is responsible for a variety of Lab duties.  The assistant is responsible for assisting in a variety of Lab duties involving the preparation, collection, documentation and shipment of PK samples for Phase 1-IV studies.   Duties and ...

    7. Clinical Analyst /Echo Sonographer

      Kelly Scientific ha a great opportunity available for an Clinical Analyst /Echo Sonographer Contract- 6 months Salary: DOEJOB REQUIREMENTS: Must have 3-5 years' experience as an echo sonographer in eco NOT ultrasound, 2 year echosonography degree, RDCS or equivalent ...

    8. Screening Manager

      Summary: The Screening Manager is responsible for overseeing the Screening. This position will ensure that the screening and panel review activity flow well together in an efficient and well-organized manner to maintain data integrity, and study participant safety.   ...

    9. Qulity Management Systems, Lead Auditor

      Summary:   The Lead Auditor will serve as the primary person responsible for executing the approved Quality Management Systems Audit plan. The Lead Auditor will service both the site-level and CRO-level operations and will report the QMS Director.   Duties and ...

    10. Quality Assurance Lead Auditior

      Summary:   The Lead Auditor will serve as the primary person responsible for executing the approved Quality Management Systems Audit plan. The Lead Auditor will service both the site-level and CRO-level operations and will report the QMS Director.   Duties and ...

    11. Clinical Research Coordinator

      The Clinical Research Coordinator (CRC) is an integral member of the core study team and serves as a point of contact for studies conducted by WCCT Global. The CRC manages and coordinates the execution of clinical trials by performing a variety of duties including but not ...

    12. Clinical Research Associate II

      Kelly Clinical Research has an exciting contract opportunity for a Clinical Research Associate II. This is a 1 year contract opportunity with the potential to extend in Irvine, CA at a medical device company.POSITION SUMMARY: Assist in preparation of clinical protocols and ...

    13. Director of Quality

      Kelly Scientific Resources, a division of Kelly Services, is actively recruiting for a Director of Quality for a major pharmaceutical company in the Orange County, CALIFORNIA area. RESPONSIBILITIES: Oversight of Quality Systems at the facility ensuring all products produced ...

    14. Clinical Programmer - Oracle Clinical

      Global medical device company is looking for a Clinical programmer to join their team in Irvine, CA. This is a 6-8 month, W-2 contract position and is open to some remote work, though candidate must be available to be on-site in Irvine on a weekly basis.   Job Description ...

    15. Director of Regulatory Affairs

        Oversees global regulatory affairs activities.  Designs, plans and executes business-aligned strategies for timely and high quality regulatory submissions in close collaboration with marketing, research and development, manufacturing, and clinical affairs partners for ...