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    1. eCTD Submissions Manager at Clinipace Worldwide

      Regulatory Affairs Certificate a plus. Minimum of eight (8) years relevant publishing experience, preferably in Pharmaceutical Regulatory Affairs....

    2. Publisher, Regulatory and Strategic Development at Clinipace Worldwide

      Regulatory Affairs Certificate a plus. The Regulatory Publisher’s charge is to manage multiple simultaneous project streams and for each, collaborate with...

    3. Director, Regulatory and Strategic Development at Clinipace Worldwide

      Create, monitor and maintain timelines for client strategic development, and regulatory affairs programs. The Director may be required to supervise and manage...

    4. Heme Tissue Bank Coordinator at University of Colorado

      E.g. Principal Investigator, Study Sponsor, FDA , PQASC , Regulatory Affairs Coordinator. UNIVERSITY OF COLORADO DENVER | ANSCHUTZ MEDICAL CAMPUS....

    5. Professional Research Assistant at University of Colorado

      E.g. Principal Investigator, Study Sponsor, FDA , Data and Safety Monitoring Committee ( DSMC ), Regulatory Affairs Coordinator....

    Ads
    1. In-House Landman III

      GOAL: Work on land and other industry related projects independently or under management direction for domestic and international oil and gas companies. Lead or collaborate on projects with internal and external teams and clients. Advise management on various Land, Legal, and Regulatory matters. Develop strategic solutions and recommend improvements to programs, processes and relationships. ...

    2. Quality_ Scientist I, AS&T

      Job Description: PURPOSE The Analytical Scientist I is responsible for the management of assigned projects. This includes the evaluation, development and validation of methods required for raw materials and finished products. Performs qualitative and quantitative analyses of organic and inorganic compounds to determine the identity, purity and homogeneity of drug substances and products ...

    3. Regulatory Affairs Specialist

        Regulatory Affairs Specialist(JOB OPPORTUNITY)-Boulder, CO  3-4 months++ PAY: OPEN DOE   Sr. Level role, more than 5 years exp required. Person needs to have Med Device experience, worked in a regulated environment and international 510K exp.   • Review all international licenses to confirm appropriate filings • Review historical product and manufacturing changes to confirm ...

    4. Regulatory Affairs Specialist

        ~~Requisition # :  49137  Assignment Information    Date Submitted :  5/26/2015 1:55:04 PM  Positions : 1  Start Date :  6/1/2015  End Date :  9/1/2015  Order Status :  Open  Order Type :  Requisition for Contract Labor  Allow receipt of resumes for :  Until Filled   Interview Type :  Phone Interview   Required Travel :  No Travel Required     Work Environment :  Professional   ...

    5. Regulatory Affairs Specialist - 137

      Regulatory Affairs Specialist - 137 3 month Contract in Boulder, CO Education Required: Graduate Degree Job Duties: Ensure compliance to the FDA Quality System Regulations, European Requirements, and other regulatory requirements. Prepare required documentation (510(k)s, technical files, dossiers) for domestic and foreign submissions and registrations. Attend design review meetings ...

    6. Medical Science Liaison - Ophthalmology

      JOB SUMMARY: Develops and maintains professional relationships with internal and external customers to provide comprehensive medical and scientific support to Client’s initiatives in assigned therapeutic areas. Facilitates information, education, and research activities for physicians and ancillary healthcare professionals regarding current and future therapies in development or ...

    7. Clinical / Biomedical Engineer

      Clinical Engineer - Medical DeviceMain Responsibilities The Senior Clinical Engineer is an R&D resource with substantial expertise in patient monitoring systems, healthcare, and knowledge of clinical environments. The Senior Clinical Engineer will participate in the creation and implementation of requirements, architecture, design documentation, software applications, test plans, development ...

    8. Director/Sr. Director

      Job Location - Novato, CA All Relocation Fees will be covered by the company.   Company is a clinical stage biotechnology company committed to bringing to market novel products for the treatment of rate and ultra-rare diseases with an initial focus on serious debilitating metabolic genetic diseases. We are launching five Phase 2 clinical trials and with another preclinical trial in the ...