• Associate Director , Global…

    Boehringer Ingelheim (Athens, GA)
    **Description** The AD Global PV Data Analysis supports the Global Pharmacovigilance (PV) team to ensure compliance with all regulations and laws worldwide on ... Pharmacovigilance (including but not limited to FDA 21 CFR,...for marketed veterinary products: + Actively participate in or lead safety surveillance and signal detection programs for Animal… more
    Boehringer Ingelheim (03/25/24)
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  • Group Medical Director

    AbbVie (North Chicago, IL)
    …safety surveillance for pharmaceutical / biological / drug -device combined products + Lead and set the strategy for key pharmacovigilance documents, including ... Instagram, YouTube and LinkedIn. Job Description Purpose: Manages other Associate Medical Directors, Medical Directors, Senior Medical Directors. Leading Product… more
    AbbVie (03/18/24)
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  • Director / (Senior) Associate

    Boehringer Ingelheim (Ridgefield, CT)
    …**_Candidate will be hired_** **_at level commensurate with experience and education._** ** Associate Director Requirements:** + US MD or DO degree or ... as required to ensure safe use in patients. The Director may also lead a team of...more than 2 years of applicable experience, required. **Sr. Associate Director Requirements:** + US MD or… more
    Boehringer Ingelheim (01/29/24)
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  • Associate Director , External…

    Lilly (Indianapolis, IN)
    …solutions to support communities through philanthropy and volunteerism. Associate Director / Director , External Collaborations will lead alliance partner ... regulatory affairs + Perform Due Diligence assessment for operational aspects for pharmacovigilance and regulatory affairs + Lead negotiations in alignment with… more
    Lilly (03/26/24)
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  • Associate Director - Patient Safety…

    Bristol Myers Squibb (Princeton, NJ)
    …medicines: The Worldwide Patient Safety group is responsible for pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety ... documents for new and expanded indications (Filing Activities). Ensures pharmacovigilance regulatory compliance. Mentors less experienced scientists and teams in… more
    Bristol Myers Squibb (04/10/24)
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  • Associate Director , Product…

    Merck (West Point, PA)
    …Product Manager - PV Signaling, Analytics & Reporting. Reporting into Product Line Lead Patient Safety, Quality & Compliance, this position will be responsible for ... managing the development and implementation of pharmacovigilance strategies, processes, and systems for a pharmaceutical company, ensuring compliance with regulatory… more
    Merck (04/18/24)
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  • Associate Director - Device Safety…

    Lilly (Indianapolis, IN)
    …and volunteerism. **Purpose:** The purpose of the Medical Device Safety Scientist Associate Director role is to leverage clinical and scientific expertise ... working across Lilly's device product portfolio to lead the completion of safety signal detection and clarification, preparation of device safety reviews, support… more
    Lilly (04/17/24)
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  • Region Associate Director / Region…

    Bristol Myers Squibb (Minneapolis, MN)
    …and spirit of independence and love of challenge. **Job Description** The Region Director (RD) is a remote leadership position that is primarily responsible for ... productivity. This position reports into a national Field Medical Director role. The RD position is underpinned with the...FM personnel (and at national level) to the FM Lead and FM Trainer; and outlines plan to address… more
    Bristol Myers Squibb (04/10/24)
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  • Associate Director or Clinical…

    AbbVie (North Chicago, IL)
    …area Medical Director or Scientific Director , the Associate Director or Clinical Scientist II, will lead the design, conduct, analysis, and reporting ... of clinical trials. The Associate Director , Clinical Science will apply scientific...related programs. * Ensure adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other… more
    AbbVie (03/18/24)
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  • Senior Associate Director , Global…

    Boehringer Ingelheim (Ridgefield, CT)
    …Medicine. You will focus on Medical Affairs, Patient Safety and Pharmacovigilance (PSPV), Regulatory Affairs, and Epidemiology. In more detail, this includes ... report audits based on a risk-based strategy in the assigned functional areas as lead auditor as well as oversee audits conducted by external auditors. + Identify… more
    Boehringer Ingelheim (03/14/24)
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  • Regional Associate Director

    Bristol Myers Squibb (Trenton, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . Position: Regional Associate Director Location: Central Region - MGG Team The Field ... insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and...FM personnel (and at national level) to the FM Lead and FM Trainer; and outlines plans to address… more
    Bristol Myers Squibb (03/21/24)
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  • Associate Director

    Lilly (Indianapolis, IN)
    …may impact a positive benefit-risk balance for a given product. The Associate Director Pharmacoepidemiology Study Operations (AD Ops)is responsible for providing ... conjunction with regulatory scientists) to identify process issues and strengths. ** Lead for department-specific operational tasks & projects** + Drive solutions… more
    Lilly (03/17/24)
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  • Associate Director , Medical Coding,…

    Boehringer Ingelheim (Ridgefield, CT)
    …and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Associate Director , Medical Coding, Analytics & Process is responsible for ... to vendor management functions and BI management. + Closely collaborates with Functional Lead Vendor Oversight in GCM to ensure awareness of coding quality and… more
    Boehringer Ingelheim (04/05/24)
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  • Director / Senior Associate

    Boehringer Ingelheim (Ridgefield, CT)
    …assigned to their program/asset. Senior CPL may assume the responsibility of an Evidence Lead in the Asset Teams, leading the creation and execution of a holistic ... of cross-functional evidence team (Clinical Operations, Biostatistics, Translational Medicine, Pharmacovigilance , Regulatory, Medical Affairs, Market Access, Epidemiology, RWE etc)… more
    Boehringer Ingelheim (02/27/24)
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  • Associate Director , Global…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data Sheets (CCDS) ... on timelines or resources, may assist another Global Labeling Lead by managing labeling development or approval for either...on timelines or resources, may assist another Global Labeling Lead by managing labeling development or approval for either… more
    Daiichi Sankyo Inc. (04/16/24)
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  • Associate Director , Informatics

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance , Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational ... governance. Responsible for Strategic Application product roadmaps to meet business objectives. Lead the definition of solutions based on business needs, cost, and… more
    Daiichi Sankyo Inc. (02/11/24)
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  • Global Safety Senior Medical Director

    Amgen (Washington, DC)
    …assigned product(s) and or setting the strategy, direction, and priorities of pharmacovigilance activities. + Manage Medical Directors, Associate Med Directors, ... you can be proud of. **Global Safety Medical Senior Director , Obesity - US Remote** **Live** **What you will...you will establish the strategy, direction, and priorities of pharmacovigilance activities and are accountable for the overall safety… more
    Amgen (04/18/24)
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  • Director Medical Affairs Psychiatry…

    Lundbeck (Deerfield, IL)
    …documents and interactions + Depending on size and needs of the team the medical director will lead , manage, coach, and develop team members (such as ... Director Medical Affairs Psychiatry - Remote Opportunity Requisition...+ Provides US medical and scientific input to the pharmacovigilance group (may serve as member of the safety...Associate Directors) to support high performance, and to align… more
    Lundbeck (03/15/24)
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  • Director CCDS Labeling Strategy

    Astellas Pharma (Northbrook, IL)
    …Labeling, Regulatory Affairs. The individual may have direct reports at the Associate Director and Manager levels. **Qualifications:** **Required** + Bachelor's ... Candidates interested in remote work are encouraged to apply. **Purpose and Scope:** The Director CCDS Labeling Strategy Lead will report to the Executive … more
    Astellas Pharma (03/15/24)
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  • Director , Rest of World Regulatory…

    Astellas Pharma (Northbrook, IL)
    …Labeling, Regulatory Affairs. The individual may have direct reports at the Associate Director and Manager levels. **Qualifications:** **Required** + Bachelor's ... work are encouraged to apply. **Purpose and Scope:** The Director ROW Labeling Lead will report to...effect decisions with local and global team members (eg, Pharmacovigilance , Medical Affairs, and affiliates members). The position reports… more
    Astellas Pharma (02/12/24)
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