Clinical Research Beginners Program
KG Hospital
Coimbatore, Tamil Nadu, IndiaFresher1h agovia LinkedIn
This job at a glance
- Who can apply
- Freshers
- Must know
- OperationsPatient careAuditingBudgeting
- Work
- On-site in Coimbatore
- Pay
- Not stated by the employer.
- Skill demand
- Patient care32%Operations18%Auditing14%Budgeting5%of 99 similar fresher jobs posted in India this week
- Listed
- 7 Nov 2026 · still open
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About the Role
This program offers an introduction to clinical research, covering 18 core areas of clinical trial operations.
Key Responsibilities & Learning Areas
- Gain knowledge of Indian and international regulatory guidelines applicable to clinical research.
- Understand clinical trial processes, including study start-up, conduct, and close-out.
- Learn informed consent procedures and documentation.
- Master source documentation, CRF completion, Source Data Verification, and Trial Master File / Investigator Site File maintenance in accordance with ALCOA+ principles.
- Develop skills in clinical trial narrative writing, including subject visit narratives, Serious Adverse Event narratives, and protocol deviation narratives.
- Understand Adverse Event Reporting, Regulatory and Judicial Submissions, follow-up activities, and the compensation claim process.
- Learn Ethics Committee submissions, documentation preparation, correspondence, and follow-up.
- Identify, document, report, and follow up on protocol deviations.
- Prepare for audits and inspections, including document preparation, query responses, and ongoing compliance maintenance.
- Coordinate monitoring visits, resolve queries, and track action items.
- Prepare, implement, assess the effectiveness of, and follow up on Corrective and Preventive Actions.
- Gain practical use of Trial Management Systems.
- Receive external certification and learning support.
- Learn the use of AI tools relevant to clinical trial operations, documentation, and workflow support.
- Understand central laboratory sample processing, handling, and shipment in accordance with the study protocol and laboratory manual.
- Learn the basics of clinical trial agreement execution and documentation, including Clinical Trial Agreements, budget agreements, Confidentiality Disclosure Agreements, and related documents.
- Engage in professional interactions and coordination with investigators, sponsors, Contract Research Organizations, vendors, central laboratories, and other laboratory facilities.
- Participate in virtual industry training programs, workshops, and professional development sessions.
Location
KG Hospital & Post Graduate Medical Institute & Research Centre, Coimbatore.