Average salary: Rs987,020 /yearly
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- ICON seeks a Pharmacovigilance Specialist to monitor pharmaceutical product safety by analyzing adverse event data, conducting signal detection, and ensuring regulatory compliance. Based in Chennai or Trivandrum, the role involves collaborating across teams to support drug ...Suggested
- ...them into technical specifications.- Develop and maintain system documentation, design specifications, configuration guides, and training... ...DORA, BaFin, and VAIT.- Experience with Archer API and Archer Control Panel for server-side administration.- Familiarity with web services...Suggested
- Senior Clinical Coding Specialist at a global CRO responsible for coding adverse events, medical histories, medications, and other clinical terminology using standard and custom dictionaries. The role involves study startup support, database coding, consistency reviews, dictionary...Suggested
- ICON seeks an Informed Consent Form Specialist to develop, review, and ensure compliance of ICFs for clinical trials across multiple India locations. The role requires expertise in regulatory guidelines, stakeholder management, and ethical conduct of research with 4–8 years...Suggested
- ...assigned topics, staying updated on changing regulatory and language requirements affecting ICFs, and developing/conducting training. Documentation and archiving: Ensuring the accuracy and completeness of ICF documents transferred for filing into the Trial Master File (TMF)....SuggestedWork at officeFlexible hours
- PV Specialist ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of ...SuggestedFlexible hours