- Merck & Co. (Rahway, NJ)
- …which operates within the larger framework of Global Regulatory Affairs, Clinical Safety , and Pharmacovigilance (GRACS), Operations, Process, & Systems (GRACS ... OPS). The RPM role sits in RPP, Portfolio and Program Management, and is one of several distinct roles that contribute to the efficient management of regulatory projects.- Position Description/Summary The RPM plays a crucial role in guiding and advancing… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core ... Data Sheets (CCDS) for assigned products. This position drives/leads the maintenance of global labeling and associated documents (including cartons and external packaging in the US) for assigned Daiichi Sankyo products. This position ensures that draft… more
- 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,...analysis of data sets as on adverse events for safety and efficacy purposes of our veterinary products. +… more
- Astellas Pharma (Northbrook, IL)
- …the pharmacovigilance function and the collection and reporting of safety information. This comprises both auditing as directed, and consultancy activities and ... risk, leading continuous improvement) services to the organization for the Pharmacovigilance and related functions. This role will coordinate the preparation, the… more
- AbbVie (North Chicago, IL)
- …signal detection, validation and assessment). Interpreting regulations related to pharmacovigilance supporting all patient safety activities. Responsibilities: + ... key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses and risk management plans + Apply current… 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
- Randstad US (Guilderland, NY)
- senior manager/ associate director , programs and digital assets. + guilderland , new york (remote) + posted 8 days ago **job details** summary + $60.30 - $70.93 ... Experience + Minimum of six (6) years of experience working within pharmacovigilance /drug safety within the biotech/pharmaceutical industry + Minimum of 1… more
- Lilly (Indianapolis, IN)
- …develop creative solutions to support communities through philanthropy and volunteerism. Associate Director / Director , External Collaborations will lead ... alliance partner relationships for Global Patient Safety (GPS) and Global Regulatory Affairs (GRA) operations and lead vendor management for GPS function. This role… 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 ... physicians in the global Inflammation Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority...more than 2 years of applicable experience, required. **Sr. Associate Director Requirements:** + US MD or… more
- Lilly (Indianapolis, IN)
- …communities through philanthropy and volunteerism. **Purpose:** The purpose of the Medical Device Safety Scientist Associate Director role is to leverage ... data sources + Consult and coordinate with the Device Surveillance Senior/Executive Director and Device Safety Physician to facilitate appropriate signal… 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 ... physicians in the global CREA Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority...years of applicable experience, required. + Leadership experience required. ** Director Requirements:** + US MD or DO degree or… more
- Merck (Rahway, NJ)
- …- 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 requirements… 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
- J&J Family of Companies (Raritan, NJ)
- …a member of Johnson and Johnson's Family of Companies, is recruiting for an Associate Director (AD), Safety Analysis Scientist (SAS), Cell Therapy to ... Research & Development, LLC is part of the Janssen Pharmaceutical Companies. The Associate Director (AD) Safety Analysis Scientist (SAS) provides scientific… more
- Boehringer Ingelheim (Ridgefield, CT)
- …within Corporate Division Medicine. You will focus on Medical Affairs, Patient Safety and Pharmacovigilance (PSPV), Regulatory Affairs, and Epidemiology. In more ... Assurance audits is to assess the audited area to ensure that the rights, safety and well-being of patients are protected, and that the integrity of data produced… more
- 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 ... the pharmaceutical industry. **Other Information/Additional Preferences:** + Experience in Pharmacovigilance and patient safety + Experience with implementation… more
- 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 ... data generation, insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on managing… more
- ThermoFisher Scientific (Wilmington, NC)
- …(comparable to 1-2 years) in the industry. + Direct experience in safety / Pharmacovigilance (comparable to 2 years). + Candidates with industry ... trial serious adverse events, marketed products ICSR and periodic safety reports ( eg PBRER, PSUR, DSUR) as well...experience(CRO/Pharma) maybe considered for Medical Director /Senior Medical Director level. _In some cases… more
- AbbVie (North Chicago, IL)
- …integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is ... key regulatory discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality… more
- Merck (Rahway, NJ)
- …which operates within the larger framework of Global Regulatory Affairs, Clinical Safety , and Pharmacovigilance (GRACS), Operations, Process, & Systems (GRACS ... OPS). The RPM role sits in RPP, Portfolio and Program Management, and is one of several distinct roles that contribute to the efficient management of regulatory projects. **Position Description/Summary** The RPM plays a crucial role in guiding and advancing… more