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regulatory affairs in Nashville

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  1. District Business Leader - Addiction - Northwest at Alkermes, Inc.

    Strong understanding of healthcare regulatory and enforcement environments and demonstrated ability to work cross-functionally....

  2. Financial Services Officer at Daymar College - Online

    Maintains a presence and active involvement in communal affairs to assure compliance with Title IV Student Financial Aid programs and all federal and state...

  3. Senior Medical Writer, Regulatory Writing at INC Research

    Management, biostatistics, regulatory affairs, and medical affairs as necessary. Adheres to established regulatory standards, including but not....

  4. Senior Medical Writer, Early Phase at INC Research

    Management, biostatistics, regulatory affairs, and medical affairs as necessary. Adheres to established regulatory standards, including but not....

  5. Regulatory Affairs Associate at N.J.S.A.

    Familiar with Regulatory regulations (e.g. Knowledge of US drug regulatory requirements. Regulatory Affairs Associate will support with new and existing...

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    1. Junior Document Control Specialist

      A leading company in the pharmaceutical industry is currently seeking a Junior Document Control Specialist to join their team. For the right candidate, this is a fantastic opportunity with great growth prospects. Details: 1) Manage the receipt, maintenance, approval, distribution, and storage of documents including non-clinical and clinical trial master files, adverse drug experiences, ...

    1. Diagnostics Liaison Manager - Tampa at AstraZeneca

      Medical Affairs Team Members. Adhere to the AZ Code of Conduct, The US Policy Handbook, Standards, and SOPs as well as comply with all regulatory and compliance...

    1. Senior Scientist

      Our client, a leading pharmaceutical company, is looking for a Senior Scientist to join their team. If you’re game for a challenge and have the required experience, this could be a great opportunity for you. 1) Draft and assist with preparation of IND and other submissions to FDA for new and existing product candidates 2) Review, organize and summarize scientific literature search, non ...

    1. Diagnostics Liaison Manager - Great Plains at AstraZeneca

      Medical Affairs Team Members. Adhere to the AZ Code of Conduct, The US Policy Handbook, Standards, and SOPs as well as comply with all regulatory and compliance...

    1. Junior Document Control Specialist

      A leading company in the pharmaceutical industry is currently seeking a Junior Document Control Specialist to join their team. For the right candidate, this is a fantastic opportunity with great growth prospects. Details: 1) Manage the receipt, maintenance, approval, distribution, and storage of documents including non-clinical and clinical trial master files, adverse drug experiences, ...

    1. Diagnostics Liaison Manager - New York at AstraZeneca

      Medical Affairs Team Members. Adhere to the AZ Code of Conduct, The US Policy Handbook, Standards, and SOPs as well as comply with all regulatory and compliance...

    1. Senior Scientist

      Our client, a leading pharmaceutical company, is looking for a Senior Scientist to join their team. If you’re game for a challenge and have the required experience, this could be a great opportunity for you. 1) Draft and assist with preparation of IND and other submissions to FDA for new and existing product candidates 2) Review, organize and summarize scientific literature search, non ...

    1. Sr Safety Specialist (United States) at INC Research

      (GCPs), regulatory guidelines, and study procedures. Evaluates AE data for completeness, accuracy and regulatory reportability....

    1. Junior Document Control Specialist

      A leading company in the pharmaceutical industry is currently seeking a Junior Document Control Specialist to join their team. For the right candidate, this is a fantastic opportunity with great growth prospects. Details: 1) Manage the receipt, maintenance, approval, distribution, and storage of documents including non-clinical and clinical trial master files, adverse drug experiences, ...

    1. Medical Editor at INC Research

      Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs in the quality review of assigned...

    1. Dir, Regulatory Strategy (United States) at INC Research

      We work with a variety of functions, including Clinical Development, Clinical Operations, Regulatory Affairs, Quality Assurance, Pharmacovigilance and Medical...

    1. Medical Science Liaison/Sr. MSL Women's Cancer I/O - Northern CA/Reno, NV at AstraZeneca

      Adhere to internal standard processes and comply with regulatory and compliance requirements. The incumbent engages in scientific information exchanges with...

    1. CA Political Director, Ecosystems at Environmental Defense Fund

      Senior Vice President, External Affairs & Communications. Extensive experience with CA state legislative and regulatory structures, and solid understanding of...

    1. Health Economics and Reimbursement Manager at KCI

      [4] various cross-functional business partners including marketing, MARCOM, Medical Affairs, Compliance, Regulatory, Legal, etc., and [5] attend trade shows,...

    1. Regulatory Affairs Coordinator at 3M

      At least 5 years in Regulatory Affairs and Documentation Activities for Medical Devices. 3M está buscando un Regulatory Affairs Coordinator para el Negocio de...

      1. Associate Medical Director at Michael J. Hennessy Associates, Inc.

        Assume role of scientific affairs lead and execute the delivery of content for 15 ancillary programs in 2016 for which funding is secured....

      2. Pharmacovigilance Associate (Men/Women) - Based in Princeton at Guerbet

        Distribute adverse event report information to Quality, Legal, Regulatory Affairs or other departments as requested by PV personnel....

      3. Associate Director, Medical Writing at Pacira Pharmaceuticals

        Regulatory medical writing experience required. The position may work closely with staff in Development Operations, Clinical Research, Regulatory Affairs,...

      4. Regional Clinical Research Associate at iCAD, Inc

        Review and collect regulatory documents and device accountability records. Accountable for data integrity, patient safety and regulatory compliance for assigned...

      5. Quality Manager, Instrument Manufacturing at Becton Dickinson & Company

        Qualifications Bachelor of Science ( BSc) or Engineering (B.Eng.), Master and/or specialization in regulatory affairs and good knowledge of molecular biology is...