Pharmacovigilance Jobs in Cambridge
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Search Results - Pharmacovigilance Jobs in Cambridge
Viridian Therapeutics-Cambridge
Overview
As the PV Operations Functional Lead, you drive pharmacovigilance execution across Viridian clinical trials and oversee vendor/CRO performance. You partner with cross-functional teams to ensure safety deliverables, regulatory compliance...
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City Therapeutics-Cambridge
Vice President, Drug Safety and Pharmacovigilance
Cambridge, MA
Vice President, Drug Safety and Pharmacovigilance
City Therapeutics is engineering the future of RNAi-based medicine. Founded by pioneers in RNA interference, we combine next...
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Sarepta Therapeutics-Cambridge
Overview
In this role you will lead global pharmacovigilance case management and oversee PV operations for Sarepta’s products. You’ll drive strategic PV projects, partner with senior management, and ensure compliant, high-quality safety data...
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City Therapeutics-Cambridge
City Therapeutics is seeking a Vice President, Drug Safety and Pharmacovigilance in Cambridge, MA to lead global safety strategy and pharmacovigilance operations. This senior medical role provides oversight of safety data, benefit-risk assessments...
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Moderna Therapeutics-Cambridge
Overview
In this role, you lead end-to-end pharmacovigilance for LATAM, ensuring regulatory compliance and PV system excellence. You’ll shape regional PV strategy, collaborate with local authorities and cross-functional teams, and oversee...
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Sarepta Therapeutics-Cambridge
Sarepta Therapeutics is seeking an Executive Medical Director, SERM to provide leadership for safety scientists and safety physicians in the SERM group. You will own safety, pharmacovigilance, and risk management activities across investigational...
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Takeda-Cambridge
Overview
In this hybrid role, you lead information governance for clinical trial records, ensuring TMF/PV documentation excellence across a global portfolio. You partner with cross-functional teams to drive inspection readiness, regulatory...
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Sarepta Therapeutics-Cambridge
Sarepta Therapeutics, headquartered in the United States, seeks an Executive Medical Director, SERM to lead safety scientists and safety physicians within PV & RM. You will own safety, pharmacovigilance, and risk management for investigational...
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GSK-Cambridge
responsibility for trials including real-time monitoring and eligibility assessment
• Review safety data with pharmacovigilance and respond to health authority queries
• Collaborate on regulatory, CMC, toxicology, and pharmacology documents; engage with ethics...
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USA - 3316 Takeda Development Center Americas, Inc.-Cambridge
JOB LOCATION:
Cambridge, MA
POSITION:
Medical Director Pharmacovigilance, Rare Disease & PDT
POSITION DESCRIPTION:
Takeda Development Center Americas, Inc. is seeking a Medical Director Pharmacovigilance, Rare Disease & PDT with the following...
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Sanofi-Aventis Deutschland GmbH-Cambridge
types of studies: long-term surveillance, compliance, pharmacovigilance, and effectiveness studies Identifies data collection opportunities during stakeholder interactions and reports these using approved processes. Maintains awareness of clinical trial...
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USA - 3316 Takeda Development Center Americas, Inc.-Cambridge
Takeda Development Center Americas, Inc. seeks a Medical Director Pharmacovigilance, Rare Disease & PDT to lead safety strategy and deliverables for assigned products. You will guide GPSE GST/SMT and interact with internal and external stakeholders...
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Planet Pharma-Cambridge
reporting and maintaining data integrity. You will collaborate with data management and safety teams to resolve reconciliation issues and provide detailed investigation notes. This position offers hands-on impact in pharmacovigilance, leveraging your...
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Sarepta Therapeutics-Cambridge
SERM will provide leadership for safety scientists and/or safety physicians in the SERM group. This individual will be accountable for safety, pharmacovigilance, and risk management activities for assigned investigational and marketed products...
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Takeda-Cambridge
and corporate obligations
• Lead cross-functional collaboration with GPL, GPM, regulatory affairs, patient safety and pharmacovigilance, and other R&D SMEs
• Drive design, execution, and interpretation of clinical studies, and oversee data analysis integration...
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