- 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,...+ Apply expertise and perform targeted data mining and product benefit-risk assessments in support of BIAH projects/products as… more
- 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
- 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
- BeiGene (San Mateo, CA)
- …departmental activities. **Supervisory** **Responsibilities:** The position has no direct reports. The Associate Director , Safety Scientist is part of a team ... 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 (Chicago, IL)
- …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
- AbbVie (North Chicago, IL)
- …Description In collaboration with a therapeutic 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 training and clinical research… 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 (Los Angeles, CA)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Summary** The Regional Associate Director (RAD) role is field-based and focused on ... 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
- 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 ... 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
- Novo Nordisk (Plainsboro, NJ)
- …current standards for safety and FDA reportability. + Serve as the back-up Pharmacovigilance responsible person for NNI. PRODUCT COMPLAINTS: + Ensures high ... FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The one thing that keeps us all marching to… more