- Merck & Co. (Rahway, NJ)
- Job Description Associate Director , Regulatory Submissions Archive Operations - Location: Rahway, NJ (Hybrid role - onsite 3 days per week required) - Functional ... (RIIM) within Global Regulatory Affairs & Clinical Safety (GRACS) - The Associate Director of Regulatory Submissions Archive Operations serves as the Business… more
- Insmed Incorporated (NJ)
- …clinical development team, partnering closely with heads of clinical operations , toxicology, regulatory affairs, commercial, pharmacovigilance , clinical quality, ... we're in. Are you?About the Role:We're looking for an Executive Medical Director of Ophthalmology, Clinical Development to help us expand what's possible for… more
- Merck & Co. (Montgomery County, PA)
- …the Pipeline Advertisemen We are currently recruiting for several Associate Director positions within US Marketing, covering Physician (HCP), Consumer (HCC), ... campaign(s) and collaborating across multiple stakeholders (including sales, marketing operations , Legal, Regulatory, Medicals, etc.) to drive promotional execution.… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- … Director is responsible for direct leadership over Grifols Biopharma pharmacovigilance and (PV) operations . Manages all adverse event investigations reported ... to perform multiple priorities efficiently and effectively. Knowledgeable of Pharmacovigilance FDA, EMEA, ICH, GMP, GCP guidelines. Demonstrated experience with… more
- Taiho Oncology (Princeton, NJ)
- …a dynamic, collaborative, and global cross-functional environment. Position Summary: The Director , Quality Assurance, ( Pharmacovigilance [PV]) reports into the ... PV and is responsible for partnering with the Sr. Director of QA, PV and PV colleagues to assure...operating procedures, as applicable. Liaise with Business Development and operations . + Provide QA support end-to-end of PV activities,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** The Associate Director , Good Pharmacovigilance Practice (GVP) Audits, serves as a key ... lead complex audits across the broader R&D, vendor, and pharmacovigilance workstreams. This position requires close collaboration with cross-functional stakeholders,… more
- Taiho Oncology (Princeton, NJ)
- …an Associate Director in PV Sciences. At the forefront of pharmacovigilance innovation, we offer a dynamic and collaborative environment where your expertise and ... with team members. + Maintain training and oversight to clinical operations / pharmacovigilance vendors supporting pharmacovigilance activities, as needed.… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **Position Overview** The Associate Director is responsible for ensuring that Primary Market Research, Competitive Intelligence, and Data ... Company policies and procedures, and governing body rules and standards. The Associate Director will: + Be a champion for ethical and compliant Primary Market… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …safety organization highly preferred. + Function as a subject matter expert in global pharmacovigilance for GPS operations and planning. + A proven ability to ... Regeneron's Global Patient Safety Organization is looking for a Director , PV Enablement to join the team!! **In this...directly to the VP of Global Patient Safety (GPS) Operations . This role is pivotal in shaping the delivery… 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 ... background check, which includes a drug screening. Our detailed, goal-oriented Pharmacovigilance colleagues manage the safety profile of new drugs in clinical… more
- CSL Behring (King Of Prussia, PA)
- …developing therapies that make a meaningful difference worldwide. Could you be our next Director , Digital Operations & Pipeline Enablement Lead ? The job is in ... establish and maintain global standards, policies, and governance frameworks for pharmacovigilance (PV) data and processes. You will create the digital… more
- BeOne Medicines (San Mateo, CA)
- The Executive Medical Director serves as the Lead Product Safety Physician for multiple or large complex strategically important developmental programs (often ... leads the incorporation of latest updates and findings from ongoing pharmacovigilance and epidemiological analysis + Actively leads BeiGene safety in face-to-face… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ensuring the quality ... compliance teams for regulations impacting Clinical, Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and procedures and determined by… more
- Boehringer Ingelheim (Athens, GA)
- …and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Director , US RA Intell. And Ext. Eng. will lead and shape Boehringer ... deputy to the Vice President, US Regulatory Affairs and Pharmacovigilance (US RAPV), this role will play a pivotal...complex regulatory issues, ensuring minimal impact on BI's business operations . + Serves as a senior advisor to internal… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Development Scientific Director **Location:** Morristown, NJ Cambridge, MA **About the Job** Join the engine of Sanofi's mission - where deep ... that could turn the impossible into possible for millions. The Development Scientific Director (DSD) is a responsible member of the clinical team dedicated to the… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …aspirations. Join Kite and help create more tomorrows. **Job Description** The Director , Medical Affairs, US Real World Evidence Center of Excellence is responsible ... to support pipeline planning as well as US safety and pharmacovigilance activities, (3) development of strategically aligned scientific publications using real-world… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring the compliance ... Quality team and share insights to trends to Clinical Pharmacovigilance and Medical Quality and R&D Quality leadership for...advancement of the Clinical Program Quality strategy, model, and operations as a key member of Clinical Quality program… more
- Ascendis Pharma (Princeton, NJ)
- …including Commercial, Legal, Regulatory, Clinical Development, Clinical Operations , Compliance, Pharmacovigilance , Biometrics, Global Communications, ... Sciences team for the US business, the Associate Medical Director supports the US Medical Director for...Associate Medical Director supports the US Medical Director for deliverables and activities associated with management and… more
- Mallinckrodt Pharmaceuticals (Bridgewater, NJ)
- Job Title Senior Medical Director - Rheumatology Requisition JR000015351 Senior Medical Director - Rheumatology (Open) Location Bridgewater, NJ Additional ... Locations Job Description Summary The Senior Medical Director , Rheumatology, will serve as a critical member of the Global Medical Affairs team. They are responsible… more
- BeOne Medicines (San Mateo, CA)
- General Description: The Senior Regional Director (SRD) (West)- Field Medical Directors (FMD) - Medical Affairs will support the National Director of the Field ... field medical team, and supporting national efforts as directed by the National Director . The Senior Regional Director will help oversee the field medical… more
