- 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 policies and procedures, quality -standards and adverse event reporting requirements internally and externally.Acts as primary site contact and site … more
- Merck & Co. (Rahway, NJ)
- …Associate Clinical Research Associate - Northeast Region (Remote) With support of Senior Clinical Research Associate (SrCRA/CRA) and/or CRA Manager , acts as ... and overall site performance.Identifies, assesses and resolves site performance, quality or compliance problems and escalates per defined CRA Escalation… more
- Integrated Resources, Inc (Atlanta, GA)
- …onsite for 1-2 days, not very often at all . Bachelor's Degree required . Pharmacovigilance experience needed . Must be flexible / adaptive . Must be able to problem ... on report Job Description: . In conjunction with the Manager of Aggregate Report Compliance and Vendor Oversight, the...including: . Office of the Chief Medical Officer (OCMO) Senior Leadership Team . Office of the QPPV .… 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
- 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
- International Rescue Committee (New York, NY)
- …N/A Other Internal and/or external contacts: * Internal:Close working relationship with Senior Manager Quality Assurance and Pharma Technical Advisors. ... Remote Job Description Additional IRC locations may be considered. Job Overview: The Senior Manager , Procurement of Medical, WASH and NFI Commodities is… 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
- Astellas Pharma (Northbrook, IL)
- …Candidates interested in remote work are encouraged to apply. **Purpose and Scope:** The Senior Manager Study Operations will mainly be asked to manage less ... **Study Manager , Evidence Generation Operations, MA-US** Do you want...of appropriate standards and processes to ensure clinical study quality + Responsible for effective training and management of… 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 april 26, 2024 **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 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
- US Tech Solutions (Raritan, NJ)
- …onsite for 1-2 days, not very often at all - Bachelors Degree required - Pharmacovigilance experience needed - Must be flexible / adaptive - Must be able to problem ... data is incorrect on report In conjunction with the Manager of Aggregate Report Compliance and Vendor Oversight, the...including: * Office of the Chief Medical Officer (OCMO) Senior Leadership Team * Office of the QPPV *… 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
- Merck (Columbus, OH)
- …**Associate Clinical Research Associate - Northeast Region (Remote)** With support of Senior Clinical Research Associate (SrCRA/CRA) and/or CRA Manager , acts as ... site performance. + Identifies, assesses and resolves site performance, quality or compliance problems and escalates per defined CRA...CRA Escalation Pathway as appropriate in collaboration with CRA Manager , CRM, TA Head and CRD as needed. +… 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
