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regulatory affairs in Nashville

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  1. Medical Writer II at INC Research

    Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing...

  2. Legislative Affairs Specialist II at American Federation of State, County and Municipal Employees

    This position serves as a primary lobbyist in the Federal Government Affairs Department. Responds to affiliate and members’ inquiries on a wide variety of...

  3. Regulatory Affairs Specialist II - Franklin TN at Wright Medical Technology, Inc.

    Implementation and management of electronic Regulatory submission processes including conversion of dossiers into the appropriate electronic format using...

  4. Medical Device Auditor / Lead Auditor / Technical Reviewer at SGS

    Global Regulatory Affairs background, including MDD / IVDD. Access and review North American clients’ medical devices quality systems and technical information...

  5. 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...

    Ads
    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. Senior Medical Science Liaison (MSL)-MO, KS, CO, NE, ND, SD at Vertex Pharmaceuticals

      Medicines Development & Medical Affairs. Assists as needed in the development of Vertex projects and initiatives with internal colleagues across functional...

    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. Field Development Agronomist - Agronomist at Arkema Americas

      Technical leadership (to include design and execution of Paladin Field R&D) within the area of expertise to Sales, Marketing and Regulatory Affairs for the U.S....

    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. Regulatory Intern 2016 at Cargill

      While working closely wit the regulatory affairs manager. This person will be responsible for responding to requests for regulatory information from internal...

    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. Vice President, Title Insurance Compliance at Altisource

      To lead the licensing, compliance, and regulatory affairs functions of the. And timely submission of regulatory reports and timely response to regulatory....

    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 Science Liaison (Southeast) at BTG Careers

      Act in accordance with applicable BTG values, and compliance, legal and regulatory requirements and code of conduct (Standard Operating Procedures-SOP)....

    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 Science Liaison, Hematology at Alnylam

      In addition, MSLs are expected to build strong cross-functional relationships with colleagues in Medical Affairs, Clinical Research, R&D, Patient Advocacy and...

    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. Agilent RA/QA QMS Lead Auditor at Agilent

      Collaborate with Agilent’s medical device regulatory experts to ensure consistent regulatory interpretations, strategies and programs....

    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. BioStatistician-C-STARS Cincinnati at BTL Technologies Inc.

      Training in human subjects’ protections, regulatory. Affairs, and data collection is highly desirable. *THIS POSITION IS CONTINGENT UPON CONTRACT AWARD**....

    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 Liaison Biopharm GHD - Rocky Mountain at Novo Nordisk

      Complies with all guidelines, policies, legal, regulatory, and compliance requirements. Understands and adheres to legal and regulatory guidelines of...

    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. Head of US Legal/Sr Corporate Counsel US/LATAM at Stratasys, Inc.

      Managing the legal affairs in North America and LATAM. Advising on, developing strategy for, and managing corporate US and regulatory compliance, dispute...

    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, ...

    2. 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, ...

    3. 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 ...

    4. 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, ...

    5. 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 ...

    6. 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 ...

    7. 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, ...

    8. 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 ...

    9. 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, ...

    10. 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 Science Liaison (MSL) – Northeast Region at ACADIA Pharmaceuticals Inc.

        Knowledge of regulatory, compliance, commercial, and clinical issues affecting the pharmaceutical and managed care industries....

      2. Sr. Medical Science Liaison (MSL) – Northeast Region at ACADIA Pharmaceuticals Inc.

        Knowledge of regulatory, compliance, commercial, and clinical issues affecting the pharmaceutical and managed care industries....

      3. Senior Medical Science Liaison (MSL)-PA, NY, WV, DE, MD at Vertex Pharmaceuticals

        Medicines Development & Medical Affairs. Assists as needed in the development of Vertex projects and initiatives with internal colleagues across functional...

      4. Medical Writer / Clinical Evaluation Report Writer at The Richmond Group USA

        Must have previous experience writing Clinical Evaluation Reports (CERs) , 4+ years of experience with Medical Writing / Documentation relating to Regulatory...

      5. Interventional Oncology Proctor at BTG Careers

        Represent the medical affairs organization in the field to reactively respond to physicians’ requests for medical information....