Clinical Trial Coordinator

Why This Role Matters

Clinical trials are essential for advancing medical science and improving patient outcomes by evaluating the safety and effectiveness of new treatments. Clinical Trial Coordinators ensure that research studies are conducted efficiently, ethically, and in compliance with regulatory standards. The Trial Coordinator position at Tata Memorial Centre offers an opportunity to support clinical research activities at a leading oncology research institution. Professionals in this role assist investigators in managing study documentation, coordinating research activities, and ensuring adherence to clinical trial protocols.
Working within a specialized oncology research environment at Homi Bhabha Cancer Hospital & Research Centre, the Trial Coordinator will contribute to the execution of clinical research studies aimed at improving cancer treatment and patient care. For candidates with a background in life sciences and clinical research training, this role offers a strong foundation for building a career in clinical trials, research coordination, and healthcare research operations.

Job Description

Tata Memorial Centre is conducting a walk-in interview to recruit a Trial Coordinator for clinical research activities at Homi Bhabha Cancer Hospital & Research Centre. The selected candidate will support clinical research studies by assisting investigators with study coordination, documentation management, and research data handling. The role involves coordinating clinical trial activities, maintaining research records, and ensuring that study procedures follow regulatory guidelines and institutional protocols. This is a contractual position with an initial tenure of six months, which may be extended based on project requirements and institutional needs.

Key Features of the Role

• Opportunity to work in clinical research within a leading oncology institution
• Exposure to clinical trial coordination and research documentation
• Involvement in patient data management and study monitoring activities
• Participation in maintaining compliance with clinical research regulations
• Opportunity to gain experience in cancer research and clinical trials

Responsibilities

Clinical Trial Coordination
Assist investigators and research teams in coordinating clinical trial activities. Support the execution of clinical research protocols while ensuring adherence to institutional and regulatory guidelines.

Study Documentation and Record Management
Maintain accurate study documentation including patient records, trial documentation, and regulatory files. Ensure proper filing and archiving of clinical trial documents.

Participant and Data Coordination
Assist in collecting and managing study-related data and maintaining patient records according to research protocols. Ensure confidentiality and proper handling of patient information.

Regulatory and Protocol Compliance
Support compliance with clinical research regulations and institutional policies. Ensure study activities align with ethical guidelines and Good Clinical Practice standards.

Collaboration with Research Teams
Work closely with investigators, clinical staff, and research coordinators to ensure efficient trial operations and timely completion of study tasks.

Required Qualifications

Educational Requirements
Candidates must have a Bachelor’s degree in Science such as B.Sc, B.Pharm, Biotechnology, Zoology, Botany, or other Life Sciences disciplines.
A Postgraduate Diploma in Clinical Research is mandatory.

Experience and Skills

Basic understanding of clinical research processes and clinical trial documentation. Strong organizational and communication skills are required for effective coordination of research activities. Candidates should demonstrate attention to detail, strong documentation skills, and the ability to collaborate with clinical and research teams.

Age Eligibility

Minimum Age Limit: 18 years
Maximum Age Limit: 35 years

Salary Insights

The selected candidate will receive a consolidated salary of ₹33,600 per month as per institutional guidelines. This role provides valuable experience in clinical research and may open opportunities for career growth in clinical trials and research operations.

Employment Details

Number of Posts: 01

The position is contractual for six months from the date of joining and may be extended depending on project requirements and institutional needs. The number of available posts may increase or decrease based on the requirements of the centre.

Interview Details

Walk-in Interview Date: 18 March 2026
Reporting Time: 09:30 AM – 10:30 AM

Interview Venue
Homi Bhabha Cancer Hospital & Research Centre
Aganampudi, Visakhapatnam – 530053
Candidates should bring their updated resume, a recent passport-size photograph, a photocopy of PAN card, original educational certificates, and one set of self-attested copies of all certificates.

Company Overview

Tata Memorial Centre is one of India’s premier cancer treatment and research organizations dedicated to advanced oncology care, clinical research, and medical education.
The institution operates specialized cancer hospitals and research centres across India, including Homi Bhabha Cancer Hospital & Research Centre, which focuses on cancer diagnosis, treatment, and clinical research. Through its clinical research programs, the centre contributes to the development of innovative cancer therapies and improves patient care through evidence-based medicine.

FAQs

Who can apply for this role?
Candidates with a Bachelor’s degree in Life Sciences such as B.Sc or B.Pharm along with a Postgraduate Diploma in Clinical Research.

Is experience required for this role?
While prior clinical research experience is beneficial, candidates with relevant education and training can apply.

What is the salary offered?
The role offers a consolidated monthly salary of ₹33,600.

Is this a permanent role?
No, this is a contractual position for six months, which may be extended depending on project requirements.

Application Tips

• Prepare an updated resume highlighting your life sciences background and clinical research training
• Clearly mention your Postgraduate Diploma in Clinical Research in the qualifications section
• Bring original certificates and self-attested copies for verification
• Highlight any internships or projects related to clinical trials or research coordination
• Arrive early at the venue to complete registration before the interview begins

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