Support clinical trial site activities and patient coordination Maintain study files, consent forms, and visit schedules Assist in data entry into EDC systems Follow ICH-GCP and protocol guidelines Coordinate with investigators and sponsors

Prepare regulatory and ethics submission documents Track site communications and documentation Support monitoring visits and audits Maintain Trial Master File (TMF) Ensure SOP compliance

Enter clinical trial data into EDC accurately and on time. Verify data against source documents. Resolve basic data queries raised by monitors or data managers. Follow data privacy and security guidelines. Support database clean-up activities.

Prepare regulatory submission documents for ethics committees and authorities. Track approval timelines and submission status. Maintain regulatory correspondence records. Support senior RA in responding to authority queries. Ensure compliance with regulatory guidelines.

Process adverse event reports from sites and investigators. Enter safety data into safety databases. Perform case triage and follow-up under supervision. Support preparation of periodic safety reports. Ensure compliance with safety reporting timelines.

Prepare, format, and manage study documents such as protocols, IBs, and SOPs. Maintain document repositories and version history. Ensure correct templates and formats are used. Support audits by retrieving requested documents. Ensure document compliance with GCP standards.

Conduct site initiation, monitoring, and close-out visits. Ensure protocol compliance and data accuracy. Train site staff on study procedures and GCP. Identify and resolve deviations, issues, and risks. Prepare visit reports and escalate concerns.

Design and manage CRFs and EDC systems. Oversee data cleaning, validation, and database locks. Define data standards and quality metrics. Manage data queries and reconciliation. Support audits and inspections.

Lead regulatory submissions and manage approvals. Interface with regulatory authorities and ethics committees. Prepare and review regulatory documentation. Track regulatory changes and ensure compliance. Support inspection readiness.

Review and analyze safety cases. Perform signal detection and risk assessment. Prepare PSURs, DSURs, and safety narratives. Ensure compliance with global safety regulations. Support inspections and audits.

Conduct internal and vendor audits. Identify compliance gaps and risks. Develop CAPA plans and track closure. Support inspection readiness. Train teams on quality standards.

Track timelines, budgets, and deliverables. Coordinate vendors, sites, and internal teams. Prepare project status reports. Identify risks and escalate to PM. Support contract and invoice tracking.

Lead clinical studies end-to-end. Manage budgets, timelines, and resources. Oversee CROs, vendors, and sites. Ensure delivery quality and compliance. Report progress to sponsors.

Define operational strategy and SOPs. Build and manage clinical operations teams. Ensure regulatory compliance and audit readiness. Drive process improvement and scalability. Manage sponsor relationships.

Define global regulatory strategy. Manage authority relationships. Lead complex submissions and negotiations. Ensure compliance across regions. Guide regulatory teams.

Latest Medical Jobs in India –
Fresher & Experienced Openings

If you are a life science graduate, pharmacy student, medical professional, or someone planning to enter the healthcare research field, this page will help you track the right opportunities at the right time.

Clinical Research Job Roles in India

Fresher Level Clinical Research Jobs

Clinical Research Coordinator

Experience- Fresher

Location- Bangalore

Job Type- Full Time

Latest Medical Jobs in India – Fresher & Experienced Openings

Clinical Research Job Roles in India

Fresher Level Clinical Research Jobs

Clinical Research Coordinator

Clinical Trial Assistant

Clinical Data Entry Associate

Regulatory Affairs Associate

Pharmacovigilance Associate

Clinical Documentation Specialist

Mid Level Clinical Research Jobs

Clinical Research Associate

Clinical Data Manager

Regulatory Affairs Executive

Pharmacovigilance Officer

Clinical Quality Assurance Auditor

Clinical Project Specialist

Senior Level Clinical Research Jobs

Clinical Project Manager

Head – Clinical Operations

Director – Regulatory Affairs

Quick Links

Useful Links

Stay Connected

Latest Medical Jobs in India –
Fresher & Experienced Openings