Associate Director, Pharmacovigilance
Holland Enterprises Inc. · Cambridge, MA
TEMPORARY
Posted Sep 10, 2026
Job Description
🚨 Now Hiring: Associate Director, Pharmacovigilance – Medical Reviewer
I’m currently looking for an experienced Associate Director, Pharmacovigilance / Medical Reviewer to join a pharmaceutical team supporting global drug safety and pharmacovigilance activities.
This is a great opportunity for an MD with strong clinical experience and pharmaceutical industry experience in medical review.
🔹 Key Responsibilities:
• Perform daily medical review and causality assessment of ICSRs
• Support signal detection and safety signal management
• Identify and escalate potential safety issues
• Collaborate with Pharmacovigilance, Case Management, Quality, and Safety teams
• Identify case review issues and inconsistencies and support resolution
• Contribute to Medical Review process improvements
• Maintain close communication with case processing and medical review vendors
🔹 Requirements:
• MD degree with at least 1 year of medical practice
• Minimum 2 years of pharmaceutical industry experience as a Medical Reviewer
• Strong clinical acumen and broad therapeutic area knowledge
• Ability to analyze and synthesize complex safety data
• Knowledge of global pharmacovigilance regulations
• Working knowledge of FDA, EU, and ICH guidelines preferred
• Excellent written and verbal communication skills
• Ability to work effectively in a fast-paced environment with tight timelines
💡 Ideal background: MD Pharmacovigilance Medical Review ICSR Causality Assessment Signal Detection Drug Safety
Interested or know someone who could be a strong fit? Feel free to message me directly!
#Hiring #AssociateDirector #Pharmacovigilance #DrugSafety #MedicalReviewer #PharmaJobs #Pharmaceutical #LifeSciences #ICSR #SignalDetection #PVJobs #DrugSafetyJobs #ClinicalSafety
I’m currently looking for an experienced Associate Director, Pharmacovigilance / Medical Reviewer to join a pharmaceutical team supporting global drug safety and pharmacovigilance activities.
This is a great opportunity for an MD with strong clinical experience and pharmaceutical industry experience in medical review.
🔹 Key Responsibilities:
• Perform daily medical review and causality assessment of ICSRs
• Support signal detection and safety signal management
• Identify and escalate potential safety issues
• Collaborate with Pharmacovigilance, Case Management, Quality, and Safety teams
• Identify case review issues and inconsistencies and support resolution
• Contribute to Medical Review process improvements
• Maintain close communication with case processing and medical review vendors
🔹 Requirements:
• MD degree with at least 1 year of medical practice
• Minimum 2 years of pharmaceutical industry experience as a Medical Reviewer
• Strong clinical acumen and broad therapeutic area knowledge
• Ability to analyze and synthesize complex safety data
• Knowledge of global pharmacovigilance regulations
• Working knowledge of FDA, EU, and ICH guidelines preferred
• Excellent written and verbal communication skills
• Ability to work effectively in a fast-paced environment with tight timelines
💡 Ideal background: MD Pharmacovigilance Medical Review ICSR Causality Assessment Signal Detection Drug Safety
Interested or know someone who could be a strong fit? Feel free to message me directly!
#Hiring #AssociateDirector #Pharmacovigilance #DrugSafety #MedicalReviewer #PharmaJobs #Pharmaceutical #LifeSciences #ICSR #SignalDetection #PVJobs #DrugSafetyJobs #ClinicalSafety
Additional Details
- City
- Cambridge
- State
- Massachusetts
- Country
- US
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