- AbbVie (North Chicago, IL)
- …Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Pharmacovigilance , Patient Safety, Epidemiology, and Quality (PSEQ) Business Process Office ... (BPOs) who are accountable for the definition, health, and performance of Pharmacovigilance 's (PV's) key end-to-end processes. The BPO partners closely with process… more
- AbbVie (North Chicago, IL)
- …to our talent pipeline and considered for future opportunities. The Associate Director (AD) of Epidemiology in Pharmacovigilance & Patient Safety leads the ... scientific strategy for pharmacoepidemiology and real-world evidence to support product development and safety across therapeutic areas. They will design and interpret studies, contribute to regulatory submissions, and provide expertise in regulatory… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Director has responsibility for pharmacovigilance risk management activities of marketed and/or investigational compounds on global level. ... position may matrix report into a Head Risk Management TA X, Global Pharmacovigilance .As an employee of Boehringer Ingelheim, you will actively contribute to the… 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
- BeiGene (Emeryville, CA)
- **General Description:** _The Associate Director , Safety Scientist supports assigned compounds in conjunction with Product Safety Leads (PSLs) and leverages ... in departmental activities **Supervisory Responsibilities:** This position has no direct reports. The Associate Director , Safety Scientist is part of a team that… more
- BeiGene (San Mateo, CA)
- **General Description:** The Associate Director of R&D Quality Systems, Strategy, and Excellence (Strategy & Innovation) is responsible for leading initiatives ... strategies that improve quality outcomes and enhance decision-making processes. The Associate Director will drive cultural change and system modernization,… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** We are looking for an experienced Associate Director , Project Manager to join our team. This successful candidate will ... across the functions (Clinical Research, Early Development, Medical Affairs, Pharmacovigilance , Regulatory Affairs) and the drug development process. + Provide… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …and any regulatory or other requirements. **This position will be filled at the Associate Director or Senior Manager level, based on experience of the identified ... projects and teams with responsibilities related to clinical trials, pharmacovigilance or other drug development activities. + Experience working with… more
- Takeda Pharmaceuticals (Lexington, MA)
- …of my knowledge. **Job Description** **About the role:** Join Takeda as an Associate Director , Market Research and Competitive Intelligence, where you will be ... and accountability on all processes related to procurement, vendors, compliance, pharmacovigilance and budget management activities in execution of each CI and… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **Job Title** : Associate Director , CPMQ Strategy and Innovation **Location** : Cambridge, MA **About ... stakeholders. + Serves as strategic thought partner to the Head of Clinical, Pharmacovigilance , and Medical Quality (CPMQ) and the CPMQ Leadership Team, driving new… more
- Vera Therapeutics (Brisbane, CA)
- Title: Associate Director , Quality Assurance Location: Brisbane, CA About Us: Vera Therapeutics (Nasdaq: VERA), is a late-stage biotechnology company focused on ... for patients suffering from immunological diseases. Position Summary: We seek an Associate Director , Quality Assurance to join an experienced, fast-paced and… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Outsourcing & Vendor Management Pleasanton, CA, USA * Princeton, NJ, USA Req #385 Friday, August 16, 2024 Looking for a chance to make a ... Proposition: Join our dynamic and expanding mid-size company in the role of Associate Director , Outsourcing and Vendor Management. Your expertise will play a… more
- Merck (Rahway, NJ)
- **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... Skills:** + Minimum 6 years' experience in Clinical Data Management or Pharmacovigilance as appropriate to business role or related industry experience preferred, at… more
- Boehringer Ingelheim (Ridgefield, CT)
- …global CNS, Retinopathy and Emerging Areas Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of our patients worldwide. ... investigational compounds. + Plan, manage / perform and monitor all pharmacovigilance activities for assigned drug responsibilities, including: + Periodic Benefit… more
- Takeda Pharmaceuticals (Boston, MA)
- …CPMQ activities eg audit, inspection, QE, CAPA. + Organise Clinical and Pharmacovigilance Quality council meetings and proactively manage the agenda and ensure key ... include successful development and implementation of a clinical or pharmacovigilance audit program, hosting/leading regulatory inspections, investigations and remediation… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **Job Title** : Associate Director , Clinical Quality Compliance **Location** : Cambridge, MA **About the ... role:** As the Associate Director , Clinical Quality Compliance, you will...Experience must include successful implementation of a clinical or pharmacovigilance audit program, hosting/leading regulatory inspections and remediation activities… more
- Lilly (Indianapolis, IN)
- …life better for people around the world. **Purpose:** The purpose of the Associate Director , Medicines Quality Organization (MQO) - Safety role is responsible ... system compliance and quality improvement of the functions he/she supports. The Associate Director is responsible for managing the quality team supporting… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …that will inspire you and empower you to shine? Join us as an Associate Medical Director Neurodegenerative Disorders in our Neuroscience Therapeutic Area Unit in ... a vital contributor to our inspiring, bold mission. **POSITION OBJECTIVES:** The Associate Medical Director leads and drives strategy for clinical studies… more
- AbbVie (Jersey City, NJ)
- …Instagram, YouTube and LinkedIn. Job Description Purpose: Manages other Associate Medical Directors, Medical Directors, Senior Medical Directors. Leading Product ... signal detection, validation and assessment). Interpreting regulations related to pharmacovigilance supporting all patient safety activities. Experts on hematology-oncology… more
- ThermoFisher Scientific (Wilmington, NC)
- …communities depend on - now and in the future. **Discover Impactful Work:** The ( Associate ) Medical Director will provide medical support and medical advice for ... clinical trials and safety evaluation within the Pharmacovigilance department. **A day in the Life:** + Provide medical leadership to the study teams, including… more
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