Karnataka

Bachelors degree in Regulatory Affairs, Science, Life Sciences, Healthcare. Author and maintain regulatory documentation including technical documentation, declarations, regulatory assessments, intended use statements, labeling reviews, and compliance records.

Your day to day interactions are with peers within Accenture. You are likely to have some interaction with clients and/or Accenture management. Accenture

In this role you are required to solve routine problems, largely through precedent and referral to general guidelines.

Review of complaints related to ExM which are received for various suppliers. Review the adequacy of investigations and coordinate with internal and external stake holders for closure.

Pharm.D or M.Pharm (Pharmacy Practice) with State Pharmacy Council registration. Prior Clinical Pharmacist experience. Department of Pharmacy Practice at JSS College of Pharmacy, Mysuru

Senior Manager CETA, you will drive Therapeutic Area performance for CDC India by providing strategic trial insights, leading portfolio planning and execution, and ensuring operational excellence across clinical trial activities.

Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures. Manage clinical and third-party data reconciliation based on edit specifications and data review plans. ICON plc

Triage and manage Requests for Information (RFI) from regulatory authorities, coordinating responses with relevant stakeholders. Collect required documents for IVDR (In Vitro Diagnostic Regulation) ethics submissions and ensure compliance with country requirements

PGs, PharmD, MPharm Pharmacology/Pharmacy Practice with some experience in clinical research and other Life Sciences PG degrees with clinical research experience. Division of Clinical Pharmacology, Department of Pharmacology, Kasturba Medical College (KMC), Manipal.