Quick overview
Job description
The Ideal Candidate:
- Analytical
- Adaptable
- Detail Oriented
- Quality-focused
What You'll Do:
- Monitor the Pharmacovigilance (PV) System through development of monthly performance reports to ensure regulatory compliance and process effectiveness.
- Prepare and analyze periodic PV metrics including KPIs, quality incidents, CAPAs, audits, and inspection outcomes.
- Compile and trend compliance data, conduct root cause assessments, gap analyses, and evaluate effectiveness of corrective actions.
- Evaluate safety reports and study documents for completeness, accuracy, and clinical relevance.
- Support audit and inspection readiness, and assist during internal audits and health authority inspections.
- Provide training on adverse event reporting and participate in internal and external meetings as needed.
- Manage safety mailbox, assess adverse event reports, and coordinate medical evaluations and escalations.
- Collaborate with cross-functional teams to enhance PV compliance activities across the organization.
- Author Safety Monitoring Plans and process adverse events in Argus database per regulatory and client requirements.
- Review and submit safety reports to regulatory agencies, resolve queries, and maintain adverse event logs.
- Conduct literature reviews for adverse event identification, reconcile AE reports with partners, and manage product complaints.
- Serve as a PV subject matter expert, support business development, train and oversee staff, and assist with resource onboarding.
What You'll Need:
- A Bachelor’s degree in a medical, nursing, pharmaceutical, or life sciences discipline is required; an advanced degree (e.g., BPharm, PharmD, RN, MD, MSc, or equivalent) is strongly preferred
- 3+ years’ experience in drug safety / pharmacovigilance in the CRO or pharmaceutical industry
- Experience in Clinical Trials and drug development (phases 1-4)
- Effective verbal and written communication skills
- Working knowledge of Argus Safety Database
- Computer literacy and proficient in Microsoft Office, particularly Word, Excel, PowerPoint
- Familiar with FDA regulations and ICH guidance
- Strong organizational skills and attention to detail
- Must possess the ability to work effectively in a fast-paced environment, and deal effectively with changing priorities
For Your Safety, Please Note:
We will never communicate with you via Microsoft Teams or text message.
We will never ask for your bank account information at any stage of recruitment.
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