- AbbVie (North Chicago, IL)
- …Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose: Manages other Associate Medical Directors, Medical Directors, Senior Medical Directors. Leading ... Product Safety Teams (PST) and supports one or more...signal detection, validation and assessment). Interpreting regulations related to pharmacovigilance supporting all patient safety activities. Responsibilities: + Understanding… more
- Boehringer Ingelheim (Ridgefield, CT)
- …**_Candidate will be hired_** **_at level commensurate with experience and education._** ** Associate Director Requirements:** + US MD or DO degree or ... accredited institution and more than 2 years of applicable experience, required. **Sr. Associate Director Requirements:** + US MD or DO degree or international… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , PV Sciences Pleasanton, CA, USA * Princeton, NJ, USA Req #361 Monday, April 22, 2024 Looking for a chance to make a meaningful difference in ... on a transformative journey with Taiho Oncology as an Associate Director in PV Sciences. At the...Director in PV Sciences. At the forefront of pharmacovigilance innovation, we offer a dynamic and collaborative environment… more
- BeiGene (San Mateo, CA)
- …in departmental activities **Supervisory Responsibilities:** The position has no direct reports. The Associate Director , Safety Scientist is part of a team that ... in this position provides safety expertise for assigned compounds with Product Safety Physician Leads (PSLs). Represents GPS department internally and externally… more
- Boehringer Ingelheim (Ridgefield, CT)
- …**_Candidate will be hired_** **_at level commensurate with experience and education._** ** Associate Director Requirements:** + US MD or DO degree or ... the global Inflammation Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of...more than 2 years of applicable experience, required. **Sr. Associate Director Requirements:** + US MD or… more
- 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...+ Consult and coordinate with the Device Surveillance Senior/Executive Director and Device Safety Physician to facilitate appropriate signal… more
- Bristol Myers Squibb (Minneapolis, MN)
- …with Neurodegenerative and Neuromuscular conditions. Bristol Myers Squibb currently markets a product in Neurology and plans to re-enter the Psychiatry market with a ... and spirit of independence and love of challenge._ **Job Description** The Region Director (RD) is a remote leadership position that is primarily responsible for… more
- Boehringer Ingelheim (Ridgefield, CT)
- …**_Candidate will be hired_** **_at level commensurate with experience and education._** **Sr. Associate Director Requirements:** + US MD or DO degree or ... the global CREA Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of...Statements + Continuous monitoring and further development of the product safety profile + Safety issue management + Set-up… more
- Lilly (Indianapolis, IN)
- …of interest which may impact a positive benefit-risk balance for a given product . The Associate Director Pharmacoepidemiology Study Operations (AD Ops)is ... Risk management is a continuous process of assessing a product 's risk and taking appropriate steps to optimize and...vendor selection decisions. + Work closely with PE Sr Director and/or delegates to identify operational gaps & drive… more
- Bristol Myers Squibb (San Francisco, CA)
- …data generation, insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on managing ... clinical trials. The RAD oversees their regional team to ensure disease and product related medical needs in the region are being identified. Oversight of the… more
- Bristol Myers Squibb (Princeton, NJ)
- …lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Established Brands Associate Director is responsible for strategy and execution of ... necessity/sensitivity assessments or other actions that require reappraisal of the product Risk/Benefit. + Partner with medical subject-matter experts from WW… more
- ThermoFisher Scientific (Wilmington, NC)
- …Functions:** Manages all medical aspects of contracted tasks across the pharmaceutical product life-cycle. **General Support:** + Ensures tasks delegated to PV are ... to 1-2 years) in the industry. + Direct experience in safety/ Pharmacovigilance (comparable to 2 years). + Candidates with industry experience(CRO/Pharma) maybe… more
- ThermoFisher Scientific (Wilmington, NC)
- …Functions:** Manages all medical aspects of contracted tasks across the pharmaceutical product life-cycle. General Support: + Ensures tasks delegated to PVG are ... (comparable to 1-2 years) in the industry; Or + Direct experience in safety/ Pharmacovigilance (comparable to 2 years). _Additional experience required for Sr Med … more
- Boehringer Ingelheim (Ridgefield, CT)
- …clinical program deliverables throughout the clinical development cycle (design of Targeted Product Profiles, preparation for the Start of Development / Release of ... of cross-functional evidence team (Clinical Operations, Biostatistics, Translational Medicine, Pharmacovigilance , Regulatory, Medical Affairs, Market Access, Epidemiology, RWE etc)… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance , Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational ... strategic vendor management relationship and governance. Responsible for Strategic Application product roadmaps to meet business objectives. Lead the definition of… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). This position ... 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data Sheets (CCDS)… more
- Amgen (Washington, DC)
- …product (s) and or setting the strategy, direction, and priorities of pharmacovigilance activities. + Manage Medical Directors, Associate Med Directors, and/or ... for a career you can be proud of. Senior Director Global Safety **Live** **What you will do** Let's...you will establish the strategy, direction, and priorities of pharmacovigilance activities and are accountable for the overall safety… more
- AbbVie (Irvine, CA)
- …of one or more clinical development programs in support of an overall Product Development Plan, based on strong medical and scientific principles, knowledge of ... and responses, and other program documents. + May oversee the work of Associate Medical and/or Scientific Directors, and of Clinical Scientists working on the same… more
- AbbVie (Mettawa, IL)
- …of one or more clinical development programs in support of an overall Product Development Plan, based on strong medical and scientific principles, knowledge of ... and responses and other program documents. + May oversee the work of Associate or Assistant Scientific Directors and of Clinical Scientists working on the same… more
- J&J Family of Companies (Horsham, PA)
- …Scientist - 2406185162W **Description** Essential Job Duties and Responsibilities The Associate Director (AD) Safety Analysis Scientist (SAS) provides scientific ... and products in development. The AD SAS will support product Safety Management Teams (SMTs) and work in close...high level of independence, with minimal guidance from the Director , Safety Analysis Scientist (SAS) Therapeutic Area Lead (TAL),… more