Senior Pharmacovigilance (PV) Clinical Scientist at ICONMA Staffing and Recruiting | Torre

Senior Pharmacovigilance (PV) Clinical Scientist

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Freelance
Recurrent
Compensation
USD50 - 57/hour
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Remote (anywhere)
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Shared by
Gabriela Enríquez Meléndez
2 days ago

Requirements and responsibilities


I'm currently partnering on an exciting opportunity for a Senior Pharmacovigilance (PV) Clinical Scientist to join a leading biopharmaceutical organization supporting critical patient safety and compliance activities.Independently lead safety case reviewsDrive compliance initiativesIdentify quality trendsAct as a Subject Matter Expert within Pharmacovigilance operationsSupport ICSR Case Processing & Clinical ReviewPerform Adverse Event (AE) AssessmentEnsure Pharmacovigilance ComplianceManage/operate within Safety DatabasesConduct Vendor Oversight & Quality ManagementContribute to SOP Development & Process ImprovementSupport Audit & Inspection activitiesParticipate in Training and MentoringWe're seeking experienced PV professionals with a Healthcare Professional Degree (PharmD, MD, RN, BSN, MSN, NP, RPh, B.Pharm, or equivalent) and a strong background in: ICSR Case Processing & Clinical Review, Adverse Event (AE) Assessment, FDA, ICH & EMA Regulations, Pharmacovigilance Compliance, Safety Databases, Vendor Oversight & Quality Management, SOP Development & Process Improvement, Audit & Inspection Support, Training and Mentoring.This role requires a professional who can independently lead safety case reviews, drive compliance initiatives, identify quality trends, and act as a Subject Matter Expert within Pharmacovigilance operations.✅ 12-Month Contract (Potential Extension) | ✅ Scientist II Level