Associate Lead
4 weeks ago
Qualification: MBBS/MD (only from Indian university)
Experience: 2 to 4 years
- Previous experience in medical review of ICSRs, Signal detection activity and aggregate safety reports.
- Knowledge of safety databases, such as Argus, ARISg, or similar systems.
- Familiarity with medical coding dictionaries (e.g., MedDRA) and adverse event reporting standards (e.g., ICH E2B).
- Strong attention to detail and ability to work with complex medical data.
- Effective communication and interpersonal skills to collaborate with cross-functional teams and stakeholders.
Key Responsibilities:
Individual Case Safety Reports (ICSRs) Review:
- Conduct thorough and objective medical review of ICSRs received from various sources, including clinical trials, spontaneous reports, and literature.
- Assess the medical relevance and causality of adverse events reported in ICSRs.
- Identify and evaluate potential safety signals and perform appropriate follow-up actions as necessary.
- Ensure accurate and timely reporting of serious and non-serious adverse events to regulatory authorities.
Aggregate and Signal Reports:
- Review and evaluate aggregate safety reports, such as periodic safety update reports (PSURs), periodic benefit-risk evaluation reports (PBRERs), development safety update reports (DSURs), CAR, and PADERs.
- Review and evaluate Signal detection reports and RMPs.
- Ensure compliance with regulatory guidelines and reporting requirements during the review of aggregate reports.
- Identify any emerging safety concerns, trends, or patterns from the aggregated safety data.
- Collaborate with cross-functional teams to contribute to risk management activities and safety signal detection.
- Authoring/review of signal detection activity
- Utilize statistical and data mining techniques to identify trends and patterns indicative of potential safety concerns. Performing validation for potential signals.
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