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Clinical Project Coordinator - Entry

Medpace
Freshers years
Not Disclosed
Mumbai, Navi Mumbai, India
15 Sept. 9, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Clinical Project Coordinator – Entry

Location: Navi Mumbai, India
Department: Clinical Trial Management
Job ID: 12947
Work Arrangement: Full-Time, Office-Based

Position Overview

Medpace is seeking a Clinical Research Project Coordinator – Entry to join its Clinical Trial Management team in Navi Mumbai, India.

This position offers an opportunity to gain hands-on experience in clinical trial management while working closely with Clinical Trial Managers, cross-functional teams, vendors, and sponsors. The successful candidate will support the coordination and execution of clinical trial activities while ensuring tasks are completed accurately and within established timelines.

Key Responsibilities

  • Support the day-to-day management of clinical trials.

  • Work closely with the Clinical Trial Manager to complete recurring project activities accurately and on time.

  • Prepare, maintain, and update project-specific status reports.

  • Maintain study information in the Clinical Trial Management System (CTMS), including milestones and enrollment projections.

  • Maintain the electronic Trial Master File (eTMF) and conduct ongoing quality checks.

  • Assist the Clinical Trial Manager with developing study plans and study-specific guidance documents.

  • Support site feasibility assessments and site activation activities.

  • Assist with clinical study supply management.

  • Coordinate effectively with regional cross-functional teams, vendors, and sponsors.

  • Participate in internal and external meetings, presentations, and conference calls.

  • Maintain a strong understanding of assigned projects and their requirements.

Required Qualifications

  • Bachelor's degree in Life Sciences or a related discipline.

  • Strong organizational and coordination skills.

  • Excellent attention to detail and accuracy.

  • Ability to manage multiple tasks and meet deadlines.

  • Good written and verbal communication skills.

  • Ability to participate confidently in internal and external meetings and conference calls.

  • Proficiency in Microsoft Word, Excel, databases, and Windows.

  • Ability to understand project requirements and coordinate activities effectively.

About Medpace

Medpace is a global, full-service Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device companies.

The organization is committed to accelerating the development of safe and effective medical treatments through high-quality clinical research. Medpace provides regulatory and therapeutic expertise across multiple areas, including oncology, cardiology, metabolic diseases, endocrinology, central nervous system disorders, and antiviral and anti-infective therapies.

Headquartered in Cincinnati, Ohio, Medpace has more than 6,500 employees across over 40 countries.

Why Work at Medpace?

Purpose-Driven Work

  • Collaborate with physicians, scientists, and clinical research professionals.

  • Contribute to the development of innovative medical therapies.

  • Support clinical research focused on improving patient outcomes.

Collaborative Work Environment

  • Work within an interactive and supportive team.

  • Participate in decision-making and problem-solving.

  • Collaborate through open communication and mutual trust.

  • Work with accessible and supportive leadership.

Learning and Career Development

  • Receive on-site mentoring in an office-based environment.

  • Follow clearly defined career development and advancement paths.

  • Participate in structured onboarding and training programs.

  • Access continuous learning and professional development opportunities.

  • Contribute ideas and take an active role in improving processes.

Benefits

  • Competitive compensation based on performance.

  • Health and wellness benefits.

  • Retirement and paid time-off benefits.

  • Office-based work environment with potential work-from-home flexibility for eligible positions after training.

  • Company-sponsored employee and social activities.

Benefits may vary depending on the country and applicable employment policies.

Ideal Candidate Profile

This position is particularly suitable for a Life Sciences graduate who is interested in building a career in clinical research and clinical trial management. The role provides practical exposure to clinical trial coordination, CTMS, eTMF, site feasibility, site activation, study documentation, clinical supplies, and collaboration with sponsors and cross-functional teams.