Pharmacovigilance jobs in United States

As our Director, you must effectively interact cross-functionally at all levels in the organization, as well as with external parties, including Regulatory Authorities, as applicable. As Director, GDS&PV Physician, you will be part of a highly skilled and international team and you will act as a ...

Dive into the dynamic world of AI and Digital Technologies at Genmab!The Role:As an Associate Digital Product Manager in IT & Digital, you will have a critical role in overseeing the product strategy, development/implementation and management of technology products in different focus areas in Glo...

Dive into the dynamic world of AI and Digital Technologies at Genmab!The Role:As an Associate Digital Product Manager in IT & Digital, you will have a critical role in overseeing the product strategy, development/implementation and management of technology products in different focus areas in Glo...

As the Associate Director, US Pharmacovigilance, you will be responsible for overall compliance of tasks within applicable regulations, SOPs, and guidelines, provide Pharmacovigilance expertise and oversight to Ferring staff and serve as PV Representative for assigned Ferring projects. ...

The PositionThe Senior Manager of Drug Safety & Pharmacovigilance (PV) Quality, is a key role and is responsible for oversight of Drug Safety & PV quality, compliance, and alliance management activities, thus always promoting inspection readiness and maintaining a robust global compliance program...

Overview:This position is to support the Global Patient Safety (GPS) department in business support of safety systems utilized for pharmacovigilance. ...

Senior Associate, Aggregate Report Compliance. Medical Safety Council Operational Compliance Committees. Other compliance review venues and for other functional partners. Minimum of 2 years of experience in pharmacovigilance case processing, aggregate reporting, and/or PV compliance monitoring. ....

Provide technical, project and administrative support to Pharmacovigilance operations teams for defined applications and tools:. Provide technical, project and administrative support to Pharmacovigilance operations teams for defined applications and tools:. ...

Consultant, GPV Case Management Product Specialist, Pharmaceuticals Summary Our growing, mid-sized pharmaceutical client has engaged GForce Life Sciences to provide a GPV Submission Specialist responsible for managing daily operational activities of the Global Submissions Team within Case process...

This job involves leadership in Drug Safety Pharmacovigilance, building and managing a Medical Safety and Risk Management team, overseeing safety and benefit-risk assessment of client's products, ensuring regulatory compliance, and collaborating with various departments in the organization. Respo...

DescriptionAscendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology.Here at Ascendis, we pride ourselves on exceptional science, visionary leader...

Reporting to the SVP, Head of Clinical Safety & Postmarketing Pharmacovigilance, the Executive Director, Postmarketing Pharmacovigilance & Compliance will play a key role in management of the Pharmacovigilance System Master File (PSMF), including Compliance and Inspection-readiness activities.  I...

DescriptionJohnson & Johnson Innovative Medicine is recruiting for an Associate Director Global Labeling Product Leader in Raritan, NJ; Titusville, NJ; Horsham, PA; Toronto, Ontario (CA); UK (High Wycombe); Netherlands (Leiden); Belgium (Beerse); Allschwil, Bern, Zug (Switzerland). At Johnson & J...

ORGANIZATION RemeGen Biosciences is a biopharmaceutical company, focusing on the discovery and development of innovative medicines for the treatment of cancer and autoimmune diseases, based in South San Francisco, California, and Rockville, Maryland. By leveraging our deep insights into oncology ...

Provide oversight of all clinical safety activities including review of medical coding of AEs, concomitant medications, and processing of SAEs through the entire lifecycle including preparation of analyses of similar events (AOSE) for unexpected and related serious adverse events (SUSARs) from cl...

- Bachelors degree in a technical field such as computer science, computer engineering or a related field required. 2-4 years experience required. Strong ability to manage and deal with different cultures and nationalities. Substantial understand...

Senior Director, Quality- GMP & GCP Location: Charlottesville, VA or San Francisco Bay Area Rivus Pharmaceuticals is searching for a Senior Director, Quality to set and lead a scalable quality strategy to advance a new class of investigational medicines called controlled metabolic accelerators (C...

Job Duties/Responsibilities: Oversight / Project Management. Understands the vendor management framework set by the Head of MAP & Safety Partnering and translates the requirements into reporting deliverables (e.g., QA/QC metrics, action items, etc.) • Works with the Vendor Lead on the oversight o...

Duration: 6 months contract, Full-Time Employment Type: W-2 Work Schedule: • Hybrid schedule 3 days onsite and 2 days remote. • Start times flexible after training. Job Description: Preferred qualification of Knowledge of FDA Quality Systems, pharmaceutical products, and Medical Device Reporting ...

Medical Director level role that provides strategic oversight for clinical development programs and associated clinical trials. Ensures the highest medical integrity and conduct of clinical studies in the execution and completion of the clinical and regulatory components of the program. Enhances ...

Apnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development...

Vice President, Drug Safety & Pharmacovigilance Company: Confidential Biopharmaceutical Company Location: Boston, MA (Hybrid, relocation required if outside 100 miles of Boston) Salary Range: $375,000 - $425,000 Reports to: Senior Vice President, Clinical Development Company Overview We are a dyn...

Senior Medical Director, Drug Safety Company – Global NASDAQ Biotech, Gene Therapy Location – Massachusetts About: Our client is a leading biotechnology company specializing in the development of gene therapy. Their focus is on creating innovative in vivo treatments that directly modify genes wit...

This candidate will collaborate with Regulatory Intelligence team, Safety Data Management to maintain accurate reporting rules in the Safety Database. Review of Pharmacovigilance Agreements and Safety Management Plans to identify new requirements and/or updates for configuration of reporting rule...