Clinical Trial Assistant Jobs at Tata Memorial Centre
Are you searching for Clinical Trial Assistant Jobs in India’s leading cancer research and healthcare institutions? Here’s an excellent opportunity from Tata Memorial Centre Careers for Life Science and Pharmacy graduates looking to enter the rapidly growing clinical research sector. This position under the National Cancer Grid Project offers hands-on exposure to clinical trials, regulatory documentation, study startup activities, and clinical research operations. If you’re looking for Life Science Jobs and a rewarding opportunity for life science graduates, this recruitment drive could be your gateway into the world of clinical research.
About Tata Memorial Centre Careers
Tata Memorial Centre is one of India’s premier cancer treatment, education, and research institutions. Operating under the Department of Atomic Energy, Government of India, the organization is internationally recognized for its contributions to oncology, clinical research, and healthcare innovation. Through Tata Memorial Centre Careers, professionals gain opportunities to work on impactful healthcare projects, clinical trials, and cutting-edge medical research initiatives. It remains a preferred destination for candidates seeking advanced Life Science Jobs and clinical research careers.
Job Details:
- Job Title: Clinical Trial Assistant
- Advertisement No.: TMC/AD/104/2026
- Organization: Tata Memorial Centre (TMC) – Tata Memorial Hospital
- Department: National Cancer Grid (NCG) Project
- Location: Mumbai, Maharashtra, India
- Employment Type: Project-Based (Initially for Six Months)
- Monthly Remuneration: ₹35,000 per month
- Application Mode: Online Only
- Application Deadline: 30 June 2026 (05:30 PM IST)
About the Role
The Clinical Trial Assistant (CTA) will provide operational, administrative, and documentation support for clinical research activities conducted under the National Cancer Grid Project. The role involves coordinating study start-up activities, maintaining essential trial documentation, supporting monitoring activities, and ensuring compliance with applicable clinical research regulations and guidelines.
The Clinical Trial Assistant serves as a key resource within the clinical research team, working closely with Clinical Research Associates (CRAs), Clinical Team Leads, Project Managers, and Finance personnel to facilitate the efficient conduct of clinical trials.
This position is ideal for life sciences, pharmacy, and clinical research professionals seeking to build a career in clinical trial management and oncology research.
Key Responsibilities
- Clinical Trial Documentation & Records Management
- Maintain, organize, and update essential clinical trial documentation.
- Ensure accurate filing and maintenance of Trial Master Files (TMFs) and study-related records.
- Support document version control and archival processes.
- Track regulatory and study-related documentation to ensure completeness and compliance.
- Study Start-Up Support
- Assist in study initiation and start-up activities for clinical research projects.
- Support preparation and coordination of study-related documentation and submissions.
- Ensure required approvals and study documents are available before study commencement.
- Coordinate communication among study teams during project initiation.
- Monitoring Support
- Provide administrative and logistical support to Clinical Research Associates (CRAs).
- Assist with planning and coordination of monitoring visits.
- Support travel arrangements and visit logistics for monitoring personnel.
- Prepare and organize documents required for site visits and audits.
- Clinical Research Operations
- Work collaboratively with Clinical Team Leads and Project Managers to support study execution.
- Monitor study-related timelines and assist in tracking project milestones.
- Support coordination among participating sites in multi-center clinical studies.
- Assist in resolving operational issues related to study documentation and coordination.
- Regulatory Compliance
- Ensure adherence to applicable clinical research regulations, ethical guidelines, and Good Clinical Practice (GCP) standards.
- Maintain confidentiality of study data and participant information.
- Support inspection and audit readiness activities.
- Ensure compliance with institutional and sponsor requirements.
- Communication & Stakeholder Coordination
- Coordinate with investigators, study coordinators, monitors, and project teams.
- Facilitate effective communication across clinical trial stakeholders.
- Maintain professional interactions with internal and external collaborators.
- Assist in scheduling meetings and maintaining study communication records.
Educational Qualifications
Essential Qualification
Candidates must possess any one of the following:
- B.Sc. in Life Sciences
- M.Sc. in Life Sciences
AND
One of the following qualifications:
- Post Graduate Diploma in Clinical Research (PGDCR)
- M.Sc. in Clinical Research
Special Eligibility
Candidates currently pursuing M.Sc. Clinical Research and completing their internship on or before 31 July 2026 are also eligible to apply.
Desirable Qualifications & Experience
- Preference will be given to candidates with:
- Experience in global clinical trials.
- Experience in multicentric clinical research studies.
- Exposure to clinical trial documentation and monitoring processes.
- Understanding of Good Clinical Practice (GCP), ICH-GCP guidelines, and clinical research regulations.
- Experience working with Clinical Research Organizations (CROs), hospitals, academic research centers, or pharmaceutical companies.
Required Skills & Competencies
- Clinical Research Knowledge
- Understanding of clinical trial processes and study life cycle management.
- Knowledge of clinical research regulations, guidelines, and documentation requirements.
- Familiarity with trial monitoring and study coordination activities.
- Communication Skills
- Excellent verbal and written communication skills.
- Fluency in English is essential.
- Ability to communicate effectively with investigators, sponsors, monitors, and research teams.
- Organizational Skills
- Strong documentation and record-management capabilities.
- Ability to manage multiple assignments simultaneously.
- Excellent time-management and prioritization skills.
- Interpersonal Skills
- Strong people-management and coordination abilities.
- Professional approach to stakeholder engagement.
- Ability to work collaboratively in multidisciplinary clinical research environments.
- Technical Skills
- Proficiency in Microsoft Office applications.
- Familiarity with clinical research databases and electronic documentation systems is desirable.
Ideal Candidate Profile
The ideal candidate is a life sciences or pharmacy graduate with formal training in clinical research and a strong interest in oncology and clinical trial management. They possess excellent organizational and communication skills, demonstrate attention to detail, and can effectively support complex clinical research projects while maintaining compliance with regulatory and ethical standards.
Candidates with exposure to multicenter studies, global clinical trials, or clinical monitoring activities will be particularly well suited for this role.
General Conditions
- The appointment is initially for a period of six months under the National Cancer Grid Project.
- Applications must be submitted through the online application portal only.
- Incomplete applications will be rejected.
- Candidates will be shortlisted based on the information provided in the online application form.
- Shortlisted candidates will be informed regarding the interview process.
- Original documents supporting educational qualifications, age, and experience must be produced at the time of the interview.
- Internal candidates must submit a No Objection Certificate (NOC) from their current Head of Department (HOD) or Principal Investigator.
- No accommodation will be provided for outstation candidates.
- Tata Memorial Centre reserves the right to modify or cancel the recruitment process without assigning any reason.
Application Process
Eligible candidates should submit their applications through the official online application portal before the deadline.
Last Date to Apply: 30 June 2026 (05:30 PM IST)
Contact Information
For recruitment-related queries:
- Telephone: 24177000 (Extension 4664)
- Email: [email protected]
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