Tata Memorial Centre Hiring Clinical Research Coordinator | Walk-In Interview 2026

If you are looking to build a career in Clinical Research and Oncology Clinical Trials, Tata Memorial Centre (TMC) has announced an excellent opportunity for aspiring Clinical Research professionals. The organization is conducting a walk-in interview for the position of Clinical Research Coordinator (CRC) under the prestigious MonarchE International Phase III Breast Cancer Clinical Trial.

This opportunity is particularly suitable for B.Pharm graduates and Science graduates who possess a Post Graduate Diploma in Clinical Research and are interested in working on international oncology studies. The role offers valuable exposure to patient management, clinical trial coordination, regulatory documentation, Good Clinical Practice (GCP), and clinical operations within one of India’s most respected cancer research institutions.

For candidates aiming to establish a long-term career in Clinical Research, this position can provide practical experience that is highly valued by CROs, pharmaceutical companies, and research organizations globally.

📌 Job Overview

🏥 About the MonarchE Clinical Trial

Selected candidates will work on the internationally recognized MonarchE Phase III Clinical Trial, a large-scale breast cancer research study evaluating the effectiveness of Abemaciclib in combination with standard endocrine therapy for patients with high-risk, node-positive, HR-positive, HER2-negative early breast cancer.

Working on such a study provides exposure to advanced oncology research methodologies, patient management strategies, clinical documentation practices, and global clinical trial standards. This experience can significantly strengthen a candidate’s profile within the clinical research industry.

💼 Key Responsibilities

As a Clinical Research Coordinator, you will play an important role in ensuring smooth execution of clinical trial activities while maintaining compliance with regulatory and ethical requirements.

• Coordinate clinical trial activities according to approved study protocols.
• Support patient recruitment, screening, and follow-up activities.
• Maintain Case Report Forms (CRFs) and study-related documentation.
• Coordinate with investigators, sponsors, monitors, and research teams.
• Manage patient scheduling and clinical study visits.
• Support Ethics Committee submissions and regulatory documentation.
• Ensure compliance with ICH-GCP guidelines and institutional SOPs.
• Assist with clinical data collection and reporting activities.
• Maintain accurate clinical trial records and audit readiness.
• Support project timelines and study milestones.

🎓 Eligibility Criteria

Candidates interested in this opportunity should meet the following requirements:

• Graduate Degree in Science OR
• B.Pharm Degree
• Post Graduate Diploma in Clinical Research (Mandatory)
• 1 Year Clinical Research Experience Preferred
• Maximum Age Limit: 35 Years

⭐ Preferred Skills

• Clinical Trial Coordination
• GCP Guidelines Knowledge
• ICH Guidelines Understanding
• Patient Management Skills
• Clinical Documentation Experience
• Regulatory Compliance Awareness
• Clinical Data Collection Knowledge
• Communication & Coordination Skills
• Problem-Solving Ability
• Attention to Detail

🌟 Why Join Tata Memorial Centre?

Tata Memorial Centre is one of India’s most respected cancer treatment and research institutions. Working at TMC offers unique exposure to oncology-focused clinical research projects and allows professionals to learn from highly experienced investigators and researchers.

• Work at a leading oncology research institute.
• Exposure to international Phase III clinical trials.
• Hands-on experience in cancer research studies.
• Government institute experience.
• Opportunity to work with renowned investigators.
• Strong clinical research learning environment.
• Professional development opportunities.

🚀 Career Growth Opportunities

Clinical Research Coordinators play a critical role in clinical trial execution and often progress into advanced positions within Clinical Research and Clinical Operations.

• Clinical Research Coordinator (CRC)
• Senior Clinical Research Coordinator
• Clinical Trial Associate (CTA)
• Clinical Research Associate (CRA)
• Senior CRA
• Lead CRA
• Clinical Trial Manager
• Clinical Project Manager
• Clinical Operations Manager

📝 Resume Tips for Clinical Research Jobs

Candidates attending the interview should ensure that their resumes highlight relevant qualifications and practical exposure.

• Mention your PG Diploma in Clinical Research prominently.
• Highlight GCP and ICH knowledge.
• Include CRC internships or research projects.
• Mention patient coordination experience.
• Include CRF handling and documentation exposure.
• Showcase regulatory documentation experience.
• Keep your resume ATS-friendly and concise.

🎯 Interview Preparation Tips

To improve your chances of selection, candidates should revise key clinical research concepts before attending the interview.

• Review GCP and ICH guidelines.
• Understand informed consent procedures.
• Study patient recruitment and retention strategies.
• Learn CRF and source documentation basics.
• Understand Ethics Committee submissions.
• Review clinical trial phases.
• Read about oncology clinical trials.
• Research the MonarchE clinical study.

📍 Walk-In Interview Details

📄 Documents to Carry

• Updated Resume/CV
• Educational Certificates
• Experience Certificates (if applicable)
• Government ID Proof
• Passport-Size Photographs
• Clinical Research Training Certificates

📢 Final Thoughts

The Clinical Research Coordinator opportunity at Tata Memorial Centre offers an excellent platform for candidates interested in oncology research and clinical trial management. Working on an international Phase III breast cancer study can provide practical exposure to global clinical research standards while helping candidates develop valuable skills in patient coordination, regulatory compliance, and clinical operations. If you meet the eligibility criteria and are passionate about clinical research, this walk-in interview is definitely worth attending.