Clinical Research Coordinator | Tata Memorial Hospital, Mumbai

Biopatrika

Mumbai

On-site

INR 274,000 - 328,000

Full time

14 days+

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Job summary

Tata Memorial Hospital in Mumbai is inviting applications for the Clinical Research Coordinator role under the RARExCAN project. The candidate will assist the PI/Co-I in screening participants, document consent, maintain study files, and manage data and reimbursements. The position is initially for six months with a monthly remuneration of ₹27,000.

Applicants should hold a B.Sc. Life Science or B.Pharm with PGDCR and possess strong communication skills.

Qualifications

  • Mandatory: B.Sc. Life Science or B.Pharm with PGDCR.
  • Desirable: experience in global and multi-centric clinical trials and good communication skills.

Responsibilities

  • Screen trial participants under the PI/Co-I supervision.
  • Document the informed consent process accurately.
  • Ensure protocol compliance across studies.

Skills

Communication skills

Education

B.Sc. Life Science
B.Pharm
PGDCR

Job description

# Clinical Research Coordinator | Tata Memorial Hospital, MumbaiJobMumbai, IndiaOctober 1, 2026Full Time### Job Overview* Date Posted October 1, 2026* Location Mumbai, India* Expiration date October 31, 2026### Job DescriptionJob Opportunity | Clinical Research Coordinator | Tata Memorial Hospital, Mumbai Tata Memorial Centre (TMC), Tata Memorial Hospital, Mumbai, has invited online applications for the post of Clinical Research Coordinator under the RARExCAN – Establishing Rare Cancer and Exceptional Responders Network in India to Accelerate Translational Research project (Project A/c No. 6354). Position: Clinical Research Coordinator No. of Posts: 01 Initial Duration: 6 months Remuneration: ₹27,000/- per month Age Limit: 27 years Qualification: B.Sc. Life Science / B.Pharm + Post Graduate Diploma in Clinical Research (PGDCR) – Mandatory Desirable: Experience in global amp; multi-centric clinical trials and good communication skills. Key Responsibilities include: • Supporting the PI/Co-I in screening trial participants • Documentation of the informed consent process • Ensuring protocol compliance • IEC communication • Data management • Maintaining Investigator Study Files • Processing participant reimbursements• Maintaining study-related trackers and logs Last Date to Apply: 02 October 2026, up to 5:30 PM IST Online Application:https://lnkd.in/d6H4P-5d Enquiry: 24177000, Ext. 4664 kevatncg.tmh@tmc.gov.in Important: Candidates should carefully review the eligibility criteria and submit their application through the official online application portal.
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