- Taiho Oncology (Princeton, NJ)
- …Value Proposition: Embark on a transformative journey with Taiho Oncology as an Associate Director in PV Sciences. At the forefront of pharmacovigilance ... have the opportunity to shape the future of drug safety , contribute to groundbreaking research, and advance patient care...experience in our rapidly evolving organization. Position Summary: The Associate Director , PV Sciences role will lead… more
- AbbVie (North Chicago, IL)
- …the direction of the Group Medical Director and Executive Medical Director in ensuring safety through surveillance, signal detection, validation, and ... assessment. Interpreting regulations related to pharmacovigilance , supporting all patient safety activities. Responsibilities: * Understands and applies… more
- Ascendis Pharma (Princeton, NJ)
- …We offer a dynamic workplace for employees to grow and develop their skills. The Associate Director , ICSR Management Team reports to the Director , Head, ICSR ... Safety Database. + Reviews and provides input to Business Partner or Pharmacovigilance Agreements and Safety Data Exchange Agreements (SDEA) to ensure… more
- ThermoFisher Scientific (Greenville, NC)
- …(comparable to 1-2 years) in the industry; Or + Direct experience in safety / Pharmacovigilance (comparable to 2 years) **For Medical Director Level:** + MD or ... comprehensive background check, which includes a drug screening. Our detailed, goal-oriented Pharmacovigilance colleagues manage the safety profile of new drugs… more
- CSL Behring (King Of Prussia, PA)
- …therapies that make a meaningful difference worldwide. We are looking for a ** Associate Director ,** **Case Management Intake & Submissions** to join our R&D ... accurate and timely entry of reports into the global safety database by the vendor. Under Case Submissions, you...schedule_ _. #LI-hybrid_ **The Role:** Reporting to the Sr. Director , Global Case Management, you will: + Oversee intake… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ensuring ... in partnership with functional compliance teams for regulations impacting Clinical, Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and… more
- Astellas Pharma (Northbrook, IL)
- …teams. 1. ** Pharmacovigilance (6 months)** + Develop hands-on experience in safety monitoring and risk management throughout the drug lifecycle. + Develop an ... diverse rotations-Clinical Development (12 months), Medical Affairs (6 months), and Pharmacovigilance (6 months), Participants will gain hands-on exposure to key… more
- Parexel (Columbia, SC)
- …broad spectrum of diseases. Overall responsibilities of the Associate / Medical Director are to: * Provide medical and safety monitoring for assigned ... expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of...needed with the support of the designated Senior Medical Director / Global Head of TA (as appropriate) Pharmacovigilance… more
- Sumitomo Pharma (Annapolis, MD)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director , Clinical Development - Oncology** . The ... associate medical director is responsible for the leadership, development, and management...NDAs, and other related documents. + Partner with Drug Safety & Pharmacovigilance to assess the … more
- Takeda Pharmaceuticals (Cambridge, MA)
- …will inspire you and empower you to shine? Join us as an Associate Medical Director , Clinical Science, Neuroscience- Pulmonologist/Neurologist in our Cambridge, ... be a vital contributor to our inspiring, bold mission. **POSITION OBJECTIVES:** The Associate Medical Director leads and drives strategy for the overall global… more
- Merck (Rahway, NJ)
- …Innovation and Information Management (RIIM) within Global Regulatory Affairs & Clinical Safety (GRACS) The Associate Director of Regulatory Submissions ... **Job Description** ** Associate Director , Regulatory Submissions Archive Operations** Location: Rahway, NJ (Hybrid role - onsite 3 days per week required)… more
- Lilly (Indianapolis, IN)
- …accountability for managing key ICSR vendor relationships. In addition, the Sr. Director leads global projects involving complex safety systems, ensuring ... and data exchange between clinical trial management systems (CTMS), safety databases, commercial pharmacovigilance platforms, and regulatory submission… more
- Gilead Sciences, Inc. (Foster City, CA)
- …individual to join the **Patient Safety Strategic Operations** team as an ** Associate Director , Patient Safety Medical Device Safety ** responsible ... strategies and ensure operational excellence through successful business partner collaboration. The Associate Director , PS Medical Device Safety will be… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …clinical pharmacology, statistics, programming, outcomes research and epidemiology, patient safety & pharmacovigilance , digital strategy, library sciences and ... sub-teams. * Be charged with integrating pharmacokinetic, pharmacodynamic, efficacy and safety data from multiple sources to optimize dosing for different… more
- Bristol Myers Squibb (Princeton, NJ)
- …(SBRA) Lead will report into the Structured Benefit-Risk Assessment Head within Safety Evidence and Sciences and will be accountable to lead structured benefit-risk ... collaboration with relevant departments across the organization, including medical safety assessment, clinical development, global regulatory, epidemiology and others.… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** Director OR Senior Associate Director has responsibility for the pharmacovigilance risk management activities of marketed and/or ... team output. + Provide updates of the assigned drug's safety profile to senior management and recommend pharmacovigilance...be an asset. + People leadership potential required. Senior Associate Director : + Total applicable experience (incl.… 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 ... responses and discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality… 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 ... 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