TMC Clinical Trial Coordinator Recruitment 2026: Walk-in Interview for Clinical Trial Coordinator Post
The Tata Memorial Centre (TMC) has invited eligible candidates to attend a Walk-in Interview for the post of Clinical Trial Coordinator. This recruitment offers an excellent opportunity for candidates interested in clinical research, healthcare management, medical research projects, pharmaceutical studies, and clinical trial operations.
The Clinical Trial Coordinator position is ideal for candidates who wish to work in a professional research environment and contribute to medical advancements through clinical studies. Selected candidates will play a crucial role in coordinating research activities, managing clinical trial documentation, supporting investigators, and ensuring compliance with research protocols.
For candidates aspiring to build a career in clinical research, healthcare research administration, and medical project management, this recruitment provides a valuable platform for professional growth.
About Tata Memorial Centre (TMC)
Tata Memorial Centre (TMC) is one of India’s leading cancer treatment and research institutions. The organization is widely recognized for its contributions to cancer care, medical research, clinical trials, healthcare innovation, and patient treatment.
TMC operates advanced facilities dedicated to:
- Cancer Treatment
- Clinical Research
- Medical Education
- Translational Research
- Clinical Trials
- Public Health Initiatives
- Oncology Research
- Healthcare Innovation
The institution regularly conducts clinical studies and research projects aimed at improving patient outcomes and advancing medical science.
TMC Clinical Trial Coordinator Recruitment 2026 Overview
Organization Name: Tata Memorial Centre (TMC)
Post Name: Clinical Trial Coordinator
Recruitment Mode: Walk-in Interview
Application Mode: Walk-in
Job Location: India
Job Category: Clinical Research Jobs
Employment Type: Contractual
Selection Process: Walk-in Interview and Document Verification
About the Clinical Trial Coordinator Position
The Clinical Trial Coordinator serves as a vital link between research investigators, healthcare professionals, study participants, and sponsors.
The role involves:
- Clinical Trial Management
- Patient Coordination
- Data Collection
- Research Documentation
- Regulatory Compliance
- Study Monitoring
- Research Administration
The position provides valuable exposure to clinical research methodologies and healthcare project management.
Educational Qualification
Candidates should possess qualifications relevant to healthcare and clinical research.
Preferred Qualifications
Applicants may possess:
- B.Sc Nursing
- B.Pharm
- Pharm.D
- Life Sciences Degree
- Biotechnology Degree
- Medical Laboratory Technology Qualification
- Clinical Research Qualification
- Master’s Degree in Relevant Discipline
Candidates with clinical research certifications may receive preference.
Experience Requirement
Relevant experience in clinical research and healthcare projects can be advantageous.
Preferred Experience Areas
- Clinical Trials
- Research Coordination
- Hospital Administration
- Patient Management
- Clinical Data Management
- Pharmaceutical Research
- Regulatory Documentation
- Research Project Support
Fresh candidates with strong academic backgrounds may also be considered depending on recruitment requirements.
Age Limit
Candidates should satisfy the age criteria prescribed by the recruiting authority.
Age Criteria
Age limits may vary according to institutional recruitment guidelines.
Age Relaxation
Applicable for eligible categories as per government and institutional norms.
Salary Structure
Selected candidates will receive remuneration according to project guidelines and institutional policies.
Benefits
- Attractive Monthly Salary
- Clinical Research Experience
- Exposure to Medical Research Projects
- Professional Development Opportunities
- Healthcare Sector Experience
- Career Advancement Prospects
The overall compensation package may vary according to qualifications and experience.
Roles and Responsibilities
Clinical Trial Coordination
Selected candidates may be responsible for:
- Coordinating clinical trial activities.
- Supporting principal investigators.
- Managing study schedules.
- Ensuring protocol compliance.
Patient Management
Responsibilities may include:
- Scheduling participant visits.
- Coordinating follow-up appointments.
- Maintaining participant records.
- Assisting during study procedures.
Documentation and Record Keeping
Clinical Trial Coordinators are expected to:
- Maintain study files.
- Prepare research reports.
- Update trial documentation.
- Manage regulatory records.
Data Collection
Candidates may assist in:
- Collecting clinical data.
- Recording study observations.
- Verifying research information.
- Supporting data management activities.
Regulatory Compliance
Responsibilities include:
- Ensuring adherence to study protocols.
- Maintaining ethical standards.
- Supporting regulatory submissions.
- Assisting audit activities.
Why Join Tata Memorial Centre?
Prestigious Healthcare Institution
TMC is one of India’s most respected cancer research and treatment centers.
Research Exposure
Candidates gain valuable experience in clinical trials and medical research.
Career Development
The position helps build expertise in clinical research and healthcare administration.
Professional Learning
Exposure to advanced healthcare systems and multidisciplinary research teams.
Networking Opportunities
Interaction with doctors, researchers, healthcare professionals, and study sponsors.
Future Career Growth
Clinical trial experience is highly valued in:
- Pharmaceutical Companies
- CROs (Clinical Research Organizations)
- Hospitals
- Research Institutions
- Biotechnology Firms
Selection Process
The recruitment process generally includes:
Walk-in Interview
Eligible candidates must attend the interview on the scheduled date.
The interview may assess:
- Clinical Research Knowledge
- Subject Understanding
- Communication Skills
- Documentation Skills
- Problem-Solving Ability
Document Verification
Candidates must produce original documents.
Documents may include:
- Educational Certificates
- Clinical Research Certifications
- Experience Certificates
- Identity Proof
- Passport-size Photographs
Final Selection
Selection may be based on:
- Educational Qualifications
- Relevant Experience
- Interview Performance
- Document Verification
Skills Required
Successful candidates should possess:
Clinical Research Knowledge
Understanding of research processes and clinical trials.
Communication Skills
Ability to interact with patients, investigators, and healthcare professionals.
Documentation Skills
Accurate maintenance of study records and reports.
Organizational Ability
Capability to coordinate multiple trial activities efficiently.
Analytical Skills
Ability to review and manage research-related information.
Teamwork
Capability to work collaboratively within research teams.
Documents Required
Candidates should carry the following documents during the walk-in interview.
Educational Documents
- Degree Certificates
- Mark Sheets
- Clinical Research Certifications
Professional Documents
- Experience Certificates
- Internship Certificates
- Training Records
Personal Documents
- Aadhaar Card
- PAN Card
- Passport-size Photographs
Additional Documents
- Updated Resume
- Identity Proof
- Category Certificate (if applicable)
How to Attend the Walk-in Interview
Step 1
Read the recruitment notification carefully.
Step 2
Verify eligibility requirements.
Step 3
Prepare all educational and professional documents.
Step 4
Update your resume with relevant qualifications and experience.
Step 5
Reach the interview venue before the reporting time.
Step 6
Complete registration formalities.
Step 7
Participate in document verification.
Step 8
Attend the interview before the selection committee.
Career Opportunities After Selection
Experience as a Clinical Trial Coordinator can open opportunities in:
Clinical Research Sector
- Clinical Research Associate (CRA)
- Senior Clinical Coordinator
- Clinical Project Manager
- Regulatory Affairs Executive
Healthcare Industry
- Hospital Research Departments
- Pharmaceutical Companies
- Biotechnology Organizations
- Medical Research Institutes
Academic and Research Careers
- Research Associate
- Project Coordinator
- Clinical Data Specialist
- Healthcare Research Professional
The experience gained through TMC significantly strengthens future career prospects.
Frequently Asked Questions (FAQs)
What is the post announced under TMC Recruitment 2026?
The recruitment is for the post of Clinical Trial Coordinator.
What is the mode of recruitment?
Selection will be conducted through a Walk-in Interview.
What qualification is required?
Candidates may possess qualifications such as:
- B.Sc Nursing
- B.Pharm
- Pharm.D
- Life Sciences Degree
- Biotechnology Degree
- Clinical Research Qualification
What is the selection process?
Selection generally includes:
- Walk-in Interview
- Document Verification
Is clinical research experience required?
Relevant experience is preferred, but eligibility depends on recruitment requirements.
Why should candidates apply?
The recruitment offers clinical research exposure, healthcare experience, professional development opportunities, and career growth in the medical research field.
Is this a good opportunity for healthcare graduates?
Yes. The position provides valuable experience in clinical trials, patient coordination, research administration, and healthcare project management.
Important Links
Official Notification: Click Here
Walk-in Interview Details: Click Here
Official Website: Click Here
The TMC Clinical Trial Coordinator Recruitment 2026 is an excellent opportunity for candidates interested in clinical research and healthcare project management. Working at Tata Memorial Centre provides exposure to advanced medical research, multidisciplinary healthcare teams, and nationally important clinical studies, making this position a strong foundation for a successful career in the clinical research industry.
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