Job Description

Work Schedule Standard (Mon-Fri)
Environmental Conditions Office

• Determine and prepare country-specific submission dossiers for DCGI & EC meeting regulatory requirements for clinical trial submissions.
• Successfully implement submission strategies to acquire regulatory and ethics committee approvals. Forecast timelines for the critical activities. Liaise with regulatory authorities and investigators to facilitate approval processes.
• Collaborate with cross-functional teams to ensure timely and accurate documentation, optimise study startup timelines.
• Obtain and review essential documents, ensure systems updation and filing.
• Monitor and ensure compliance with local and international regulations.
• Work and drive the amendments and support the ongoing submissions, notifications for the ongoing studies.
• Provide guidance and support to project teams on local regulatory and GCP requirements, timelines and strategy.

Skills Required