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regulatory affairs in Nashville

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  1. Technical Service Manager at Kemin Industries, Inc.

    Ability to work in cross-functional teams to achieve customer and product objectives, including R&D, Regulatory Affairs and Operations....

  2. Program Manager (Regulatory Affairs) at PAREXEL International

    Acts independently in a client-facing role Provides a full range of consulting services and works within their personal area of expertise Takes responsibility...

  3. Senior Manager, Knowledge Management for Medical Affairs at Chiltern

    Knowledge of regulatory requirements and clinical data systems preferred. The position will collaborate with teams within medical affairs, IT and other groups...

  4. INTERNATIONAL STUDENT COORDINATOR at Central Michigan University

    Master’s degree in International Education, Educational Leadership, Student Affairs or related field....

  5. 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...

    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. Interventional Oncology Proctor at BTG Careers

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

    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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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 ...

    3. 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, ...

    4. 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 ...

    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. 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, ...

    7. 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 ...

    8. 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, ...

    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. 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...

      2. 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...

      3. 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...

      4. 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....

      5. 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....