SME_Pharmacovigilance (Bengaluru)

SME_Pharmacovigilance (Bengaluru)

16 Oct
|
Orcapod Consulting Services
|
Bengaluru

16 Oct

Orcapod Consulting Services

Bengaluru

Key Responsibilities:

- Handle and review adverse event/safety case reports.

- Perform ICSR processing and ensure accurate case documentation.

- Review patient, drug, and adverse event information.

- Perform medical coding and case assessment as per applicable guidelines.

- Support case quality checks and ensure compliance with SOPs and regulatory requirements.

- Identify and escalate discrepancies or missing information.

- Support the team in meeting quality and productivity targets.

- Provide SME-level guidance to team members and support process-related queries.

Preferred candidate profile

- 1+ year of relevant Pharmacovigilance experience

- Valuable understanding of ICSR / Adverse Event case processing

- Knowledge of safety databases and PV processes

- Good communication and analytical skills

- Ability to work as per process requirements/shifts, if applicableRole & responsibilities

📌 SME_Pharmacovigilance (Bengaluru)
🏢 Orcapod Consulting Services
📍 Bengaluru

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