- Merck & Co. (Rahway, NJ)
- …for assigned protocols and sites in a country.Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country ... regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and...and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study,… more
- Takeda Pharmaceuticals (Lexington, MA)
- …my knowledge. **Job Description** Takeda Development Center Americas, Inc. is seeking a Senior Manager , Pharmacovigilance (PV) Business Partner Relations in ... of related experience. Required skills: Review and provide input on Pharmacovigilance Agreements (PVAs) and associated business agreements; analyze and provide… more
- BeiGene (Emeryville, CA)
- …departmental activities **Supervisory Responsibilities:** + The position has no direct reports. The Senior Manager , Safety Scientist is part of a team that ... + Assist with integrated Benefit/Risk assessments **Promote and Advance the Field of Pharmacovigilance ** + Any other tasks assigned by manager to assist in… more
- Regeneron Pharmaceuticals (Armonk, NY)
- The Senior Manager , Global Development Quality Management (GCP) acting as a Quality Management Lead (QML) is a key position that will provide mentorship ... and leadership for all aspects of quality and compliance. The incumbent will engage with key...transferable skills related to Good Clinical Practice(GCP), and/or Good Pharmacovigilance Practice (GVP). Does this sound like you? Apply… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …on real-world evidence, and creating hope for all facing illness. The Senior Managerwill support signal detection activities and medical analyses to support ... with Drug Safety Global Safety Team (GST) Chair (Medical Director). The Manager , MSE will perform signal management process activities for assigned products,… more
- Sanofi Group (Cambridge, MA)
- …treatment to patients with specific illnesses where treatment access is limited. **Global Senior Manager - Governance & Risk Management** sits within Specialty ... EAP programs management. + Significant experience in Medical Governance, Medical Quality , Pharmacovigilance , Regulatory Affairs, Medical Operations (at global… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …to the best of my knowledge. **Job Description** **Job Description for Senior Medical Director, Clinical Science, Marketed Products Development** As the Senior ... and partners with marketed products R&D function leads (regulatory affairs, pharmacovigilance , global development operations and project management) to set R&D… more
- Boehringer Ingelheim (Ridgefield, CT)
- …etc.). Senior CPL will liaise with the Digital Content Manager regarding new tools/technologies/best practices. + Provides input into Medical Affairs strategy ... **Description** The role of Senior Clinical Program Leader (CPL) - Retinal health,...The incumbent will drive patient value, patient voice and quality of life & outcomes in line with Medicine… more
- Randstad US (Cambridge, MA)
- senior safety associate iii. + cambridge , massachusetts + posted 9 days ago **job details** summary + $50.72 - $57.58 per hour + contract + bachelor degree + ... 57.58 per hour work hours: 9 to 5 education: Bachelors responsibilities: The Senior Safety Associate III will be responsible for supporting Global Case Management… more
- Merck (Columbus, OH)
- …for assigned protocols and sites in a country. Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country ... regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and...and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study,… more
- Merck (Columbus, OH)
- …Lead {CQOL and Head of Clinical Quality Operations (HCQO), the Clinical Quality Operations Manager (CQOM)} is responsible for the execution of operational ... **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide the safety...indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying… more
- Pfizer (Tampa, FL)
- **Role Summary** The Audit Manager , Research, Development and Supply will be part of Pfizer Corporate Audit's internal team that provides "third line of defense" ... Chain to plan and execute best in class audit assurance. The Audit Manager is responsible for identifying risks in specific business areas and conducting independent… more
- AbbVie (Boston, MA)
- …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Manager of Safety Statistical Programming is a strategic role in the emerging ... of integrated clinical safety data for multiple compounds and indications. The Manager of Safety Statistical Programming must effectively interface with team members… more
- Bristol Myers Squibb (Chicago, IL)
- …and payers. The RD position is also responsible for working closely with senior management to create and execute medical initiatives at a national level. This ... leadership commitment and role modelling of the highest standards of quality , compliance, uncompromising ethics and integrity. **Leading and Managing Field Medical… more
- Boehringer Ingelheim (Ridgefield, CT)
- …among team members, encourage cross-functional coordination and coordinate with the ( senior ) regulatory project manager to achieve regulatory milestones & ... apply to, or be accessible to any company recruiter worldwide. Given that the hiring manager is not based in the country you are applying for and the interview… more
- AbbVie (North Chicago, IL)
- …Strategy Teams (CSTs) and clinical study teams, to ensure high- quality , cross-functionally-aligned program (ie, Clinical Development Plan) and study deliverables ... strategies at a disease area and platform level. + Acts as a senior -level liaison for opinion leader interactions related to the disease area(s); partners with… more
- Editas Medicine (Cambridge, MA)
- …messaging and communication strategies. The incumbent is expected to be a strong people manager and be willing to 'roll up the sleeves' as needed to accomplish ... pre-IND activities to BLAs, establishing plans for long-term follow up and pharmacovigilance , and is responsible for protocol development and clinical sections of… more
