Clinical Trial Coordinator

16 hours ago

Chennai, Tamil Nadu, India ClinoGenesis Research Institute Full time ₹ 2,50,000 - ₹ 4,00,000 per year

Clinical Trial Coordinator (CTC)

Location:
[Insert City / Across India – Hybrid / On-site]

Organization:
Clinogenesis Research Organization

Department:
Clinical Operations

Employment Type:
Full-Time

About Clinogenesis

Clinogenesis Research Organization is a rapidly growing, innovation-focused CRO dedicated to advancing high-quality clinical research and data-driven healthcare solutions. We are committed to training and developing fresh talent, offering a strong foundation for those aspiring to build a successful career in the clinical research industry.

About the Role

We are seeking an enthusiastic and detail-oriented Clinical Trial Coordinator (CTC) to support our clinical operations team in the management and execution of ongoing clinical trials. This is an excellent opportunity for freshers or early-career professionals to gain hands-on experience in study coordination, documentation, and site communication.

Key Responsibilities

Assist in the planning, coordination, and tracking of clinical trial activities.

Support site initiation, routine monitoring preparations, and close-out activities.

Maintain and update Trial Master File (TMF) and Investigator Site File (ISF).

Coordinate with investigators, site staff, CRAs, and internal teams to ensure smooth trial operations.

Assist with regulatory submissions, ethics committee documentation, and study approvals.

Track subject enrollment, visit schedules, and study progress metrics.

Support preparation of reports, meeting minutes, logs, and study trackers.

Ensure compliance with ICH-GCP, SOPs, and protocol requirements in all study-related activities.

Qualifications

Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, Biotechnology, or related fields.

0–1 year of experience in clinical research (freshers encouraged to apply).

Basic understanding of clinical trial processes, regulatory guidelines, and GCP principles.

Strong organizational abilities, communication skills, and attention to detail.

Proficiency in MS Office (Excel, Word, PowerPoint).

Ideal For

Fresh graduates looking to begin a career in clinical research

Candidates interested in study coordination and clinical operations

Individuals who are detail-oriented, proactive, and eager to learn

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