Pharmacovigilance Jobs in Cambridge
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Search Results - Pharmacovigilance Jobs in Cambridge
Stratacuity: Proven Scientific Placement-Cambridge
Primary Job Requirements:
• MD with 10+ years of experience in drug development and drug safety/pharmacovigilance, with specific expertise in clinical oncology, immunology, or genetics
• Strong knowledge and hands-on experience with good pharmacovigilance...
mindmatch.ai -
Biogen-Cambridge
Job Description
What you’ll do:
The Associate Medical Director, Global Safety Physician will be responsible for global pharmacovigilance for investigational and/or marketed products, including review and analysis of safety data, design of clinical...
resume-library.com -
TalentBurst, an Inc 5000 company-Cambridge
of late-stage clinical trials.
• Under the guidance of the CRD he/she collaborates with the Coding specialist, Biostatisticians, Data Managers, Global and Regional Study Managers, Feasibility Managers, Pharmacovigilance representative, Medical Writer (e.g...
mindmatch.ai -
Aequor Technologies LLC-Cambridge
Study Managers, Feasibility Managers, Pharmacovigilance representative, Medical Writer (e.g. planning and review of narratives) on high quality medical review, as needed. He/she supports the CRD to ensure appropriate documentation and consistency...
resume-library.com -
ONO PHARMA USA-Cambridge
and understanding of clinical development in various therapeutic areas, the impact of pharmacologic agents on humans, nonclinical (toxicology) and regulatory requirements for testing new therapies in humans.
• Possesses proficiency with pharmacovigilance programs...
mindmatch.ai -
Bicycle Therapeutics-Cambridge
including but not limited to vendor audits and maintenance of preferred vendor list)
Provide expert quality consultation to stakeholders (e.g., Clinical Operations, Data Management, Pharmacovigilance, etc.) based on analysis and interpretation of applicable...
resume-library.com -
Randstad-Cambridge
functions with oversight from the product-specific Global Safety Officers.
• support for global pharmacovigilance of assigned products as needed, including the review and analysis of safety data from clinical studies, the post-marketing setting...
randstadusa.com -
Biogen-Cambridge
Job Description
About This Role
The Medical Director, Drug Safety is responsible for global pharmacovigilance for marketed and/or investigational products, including review and analysis of safety data from post-marketing sources and from clinical...
resume-library.com -
Apnimed-Cambridge
Communications team
• Collaborate with Pharmacovigilance and Quality teams to design and execute intake and processing of AE and PQC case reports
• Supports MLR review process for internal and external medical and commercial materials
• Ensure best practices...
mindmatch.ai -
Randstad-Cambridge
in a team environment
skills: Pharmacovigilance, MS-WORD, MS-EXCEL, MS-Powerpoint, ICSR (Individual Case Study Report)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information...
randstadusa.com -
LanceSoft Inc-Cambridge
Remote EST, 8-5pm
Provides regulatory expertise and guidance to Clinical, Pharmacovigilance, Legal, Scientific, Commercial, and other internal stakeholders for successful development of Company Core Data Sheets (CCDSs) and global labeling, i.e., US...
resume-library.com -
Randstad-Cambridge
Feasibility Managers, Pharmacovigilance representative, Medical Writer (e.g. planning and review of narratives) on high quality medical review, as needed. He/she supports the CRD to ensure appropriate documentation and consistency of the data...
randstadusa.com -
eTeam Inc.-Cambridge
Study Managers, Feasibility Managers, Pharmacovigilance representative, Medical Writer (e.g. planning and review of narratives) on high quality medical review, as needed. He/she supports the CRD to ensure appropriate documentation and consistency...
resume-library.com -
TalentBurst, Inc.-Cambridge
are coordinated and consistent
Provide relevant clinical scientist expertise to internal teams, including clinical operations, medical writing, biostatistics, data management, and pharmacovigilance to ensure quality processes and deliverables
Development...
resume-library.com -
Editas Medicine-Cambridge
responsibility for conceiving, delivering, and overseeing Phase 1-3 trials progressing from pre-IND activities to BLAs, establishing plans for long-term follow up and pharmacovigilance, and is responsible for protocol development and clinical sections...
resume-library.com -
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