TMC Research Project Manager Recruitment 2026
Project: MK3475-593 / KEYNOTE-593
Pembrolizumab (KEYTRUDA®) Safety Study in Melanoma and PD-L1 Positive NSCLC — India
Advertisement No.: TMC/AD/179/2026
Post: Research Project Manager
Project A/c No.: 4386
Engagement: Initially for a period of six months
Location: Tata Memorial Hospital, Mumbai
Online Application Deadline Countdown
Online applications close on 12 November 2026. Verify the exact closing time on the official TMC Careers page.
1. Recruitment Overview
Vacancy clarification: The recruitment listing for TMC/AD/179/2026 does not specify the number of posts. Candidates should refer to the detailed official notice on the TMC Careers portal for any clarification.
2. Important Dates and Timings
| Event | Date / Time |
|---|---|
| Online applications open | 04 November 2026 |
| Last date for online application | 12 November 2026 |
| Tenure | Initially for a period of six months |
| Interview / selection date | Not specified in the available listing |
3. Post and Project Details
| Post | Project | Study Code | Location | Tenure |
|---|---|---|---|---|
| Research Project Manager | MK3475-593: A Prospective, Open-label, Phase 4 Study to Evaluate the Safety of Pembrolizumab (KEYTRUDA®) in Subjects with Unresectable or Metastatic Melanoma or PD-L1 Positive Non-small Cell Lung Cancer (NSCLC) in India | KEYNOTE-593 Project A/c No. 4386 |
Tata Memorial Hospital, Mumbai | Initially six months |
The post is advertised under Project Posts for a specific clinical research study. The engagement is initially for a period of six months and is subject to the project's requirements and official terms.
4. Educational Qualification
Qualification not specified in the available listing
The short recruitment listing for TMC/AD/179/2026 does not state the essential educational qualification, experience or technical requirements for the Research Project Manager post.
- Refer to the detailed official notice on the TMC Careers portal for the exact qualification and experience requirements.
- Keep degree certificates, mark sheets and experience letters ready for verification.
- Clinical research project management roles commonly require relevant experience, but eligibility must be confirmed only from the official notice.
- Do not assume eligibility based on this article — the selection committee will apply the official criteria.
5. Age Limit and Relaxation
Age limit: Not specified in the available listing.
| Category | Age Relaxation stated in listing |
|---|---|
| All categories | Not specified — verify from the official notice |
Project posts may follow specific age conditions mentioned in the detailed notice. Candidates should confirm the applicable age limit and the cut-off date for age calculation from the official TMC notice.
6. Salary and Remuneration
Remuneration not disclosed in the available listing
The listing does not mention the monthly remuneration or consolidated pay for the Research Project Manager post. Remuneration will be as per the official notice and the project's terms.
- Project posts are generally paid a consolidated amount as per the sanctioned project budget.
- The detailed notice usually specifies whether any allowances or deductions apply.
- Candidates should clarify remuneration and service conditions during the selection process.
7. Tenure and Nature of Appointment
- The engagement is initially for a period of six months.
- The post is listed under Project Posts, not a regular permanent appointment.
- The engagement is linked to the study MK3475-593 / KEYNOTE-593 and Project A/c No. 4386.
- Extension or continuation, if any, will be governed by project requirements and institutional terms.
- Appointment conditions and joining formalities will be as per TMC's applicable rules.
8. About the Study — KEYNOTE-593
The advertised post is for a prospective, open-label, Phase 4 study evaluating the safety of Pembrolizumab (KEYTRUDA®) in subjects with unresectable or metastatic melanoma or PD-L1 positive non-small cell lung cancer (NSCLC) in India.
Pembrolizumab is an immune checkpoint inhibitor used in certain cancers. Phase 4 studies are conducted after a medicine has received regulatory approval and focus on safety, real-world use and broader clinical experience. A Research Project Manager in such a study typically supports study coordination, documentation, regulatory compliance, site communication and project timelines.
General Areas Relevant to a Research Project Manager
The following are general areas relevant to clinical research project management. Actual duties will be determined by the department and the study protocol:
- Overall coordination of study activities at the site.
- Tracking project timelines, deliverables and milestones.
- Supporting ethics committee and regulatory submissions.
- Maintaining study files, essential documents and records.
- Coordination with investigators, study staff and sponsors.
- Monitoring patient enrolment and data collection progress.
- Supporting pharmacovigilance and safety reporting workflows.
- Ensuring compliance with protocol, GCP and institutional policies.
- Preparing project reports and documentation for review.
- Coordinating audits, monitoring visits and quality checks.
9. Suggested Interview Preparation Topics
A. Clinical Research Fundamentals
- Phases of clinical trials, including Phase 4 studies.
- Principles of Good Clinical Practice (ICH-GCP).
- Informed consent process and participant rights.
- Role of ethics committees and regulatory authorities.
- Essential documents and study file maintenance.
- Protocol compliance and deviations.
B. Project Management in Clinical Research
- Study start-up, conduct and close-out activities.
- Timeline planning and milestone tracking.
- Budget tracking and project documentation.
- Risk identification and issue escalation.
- Coordination between sponsor, site and study team.
- Preparing for monitoring visits and audits.
C. Oncology and Study-Specific Awareness
- Basic understanding of melanoma and NSCLC.
- Role of immunotherapy and checkpoint inhibitors.
- Pembrolizumab (KEYTRUDA®) — general mechanism and safety monitoring concepts.
- Adverse event and serious adverse event reporting basics.
- Patient safety and pharmacovigilance workflows.
- Importance of protocol-defined assessments.
D. Data Management and Documentation
- Source documentation and case report form basics.
- Data quality, accuracy and completeness.
- Confidentiality and patient data protection.
- Record retention and document control.
- Query resolution and follow-up.
Suggested Professional Interview Questions
- What is the difference between Phase 3 and Phase 4 clinical studies?
- What are the core principles of ICH-GCP?
- How do you manage study timelines when multiple sites are involved?
- What documents are part of the essential study file?
- How would you prepare a site for a monitoring visit?
- What is the process for reporting a serious adverse event?
- How do you ensure protocol compliance by the study team?
- What is your experience with ethics committee submissions?
- How do you handle a delay in patient enrolment?
- What do you understand by Pembrolizumab and its safety monitoring?
10. Selection Process
The available listing states that online applications are invited. It does not publish a separate written examination or detailed selection schedule.
- Check the official notice and confirm eligibility.
- Complete the online application on the TMC Careers portal before the last date.
- Keep all academic and experience documents ready for verification.
- Shortlisted candidates will be informed as per TMC's process.
- Attend the interview or selection process as directed by TMC.
- Final selection will be subject to institutional assessment and verification.
11. Documents Required
Prepare the following documents for the online application and any later verification:
- Updated CV / Resume.
- Photo ID proof.
- Educational qualification certificates and mark sheets.
- Experience certificates from previous employers, if any.
- Category certificate, if applicable.
- Any registration or licence required for the post, if applicable.
- Recent passport-size photograph.
- Any additional documents requested in the official notice.
12. How to Apply Online
- Open the TMC Careers portal.
- Locate advertisement number TMC/AD/179/2026.
- Read the full official notice and confirm eligibility.
- Register or log in as required on the application portal.
- Fill in the online application form carefully.
- Upload the required documents and photograph.
- Review the application and submit it before 12 November 2026.
- Save the submitted application or acknowledgement for future reference.
13. Application Fee
The available listing does not mention an application fee. Candidates should check the official notice and should never pay money to agents or unauthorized persons for application, selection or appointment.
14. Important Official Links
15. Frequently Asked Questions (FAQs)
Tata Memorial Centre, Tata Memorial Hospital, Mumbai.
TMC/AD/179/2026.
Research Project Manager under Project A/c No. 4386.
MK3475-593 / KEYNOTE-593 — a Phase 4 study evaluating the safety of Pembrolizumab (KEYTRUDA®) in patients with unresectable or metastatic melanoma or PD-L1 positive NSCLC in India.
The number of vacancies is not specified in the available listing. Refer to the official notice.
The qualification requirement is not stated in the available listing. Candidates must check the detailed official notice.
Remuneration is not disclosed in the available listing. It will be as per the official notice and project terms.
The age limit is not specified in the available listing. Verify from the official notice.
The engagement is initially for a period of six months.
Apply online through the TMC Careers portal. The application window is from 04 November 2026 to 12 November 2026.
No application fee is mentioned in the available listing. Check the official notice for confirmation.
No. It is a Project Post for an initial period of six months, subject to project requirements and institutional terms.
