Clinical Project Coordinator - Entry

Medpace Clinical Research India; Mumbai; On-site; INR 300,000 - 420,000; Full time

Job summary

Medpace Clinical Research India in Navi Mumbai, India, seeks a full-time Clinical Research Project Coordinator at an entry level for an office-based role. You will join a Clinical Trial Management team to support daily trial activities and coordinate with cross-functional partners.

The position offers an opportunity to develop expertise in trial management, CTMS/eTMF processes, and study planning while advancing your career within a global CRO.

Qualifications

• Bachelors degree in a life sciences field.
• Maintain thorough knowledge of project and ability to coordinate/present at internal/external meetings and conference calls.
• Excellent computer (word-processing, databases, Excel, Windows) and organizational skills.

Responsibilities

• Engage in clinical trial management on a day to day level.
• Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy.
• Compile and maintain project-specific status reports.
• Update CTMS with study milestones, enrolment projections etc.
• Update eTMF and perform ongoing eTMF QC.
• Support clinical trial manager to draft study plans and study specific guidance documents.
• Manager site feasibility, site activation preparation and study supply managements.
• Communicate with regional cross functional team, vendors and sponsor effectively.

Skills

Coordination & presentation

Computer skills

Organizational skills

Education

Bachelors degree in life sciences

Job description

Job Summary

We are currently seeking a full-time, office-based Clinical Research Project Coordinator Entry to join our Clinical Trial Management team in Navi Mumbai, India. This position will work on a team to accomplish tasks and projects that are instrumental to the company s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

• Engage in clinical trial management on a day to day level;
• Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy;
• Compile and maintain project-specific status reports;
• Update CTMS with study milestones, enrolment projections etc.
• Update eTMF and perform ongoing eTMF QC;
• Support clinical trial manager to draft study plans and study specific guidance documents;
• Manager site feasibility, site activation preparation and study supply managements;
• Communicate with regional cross functional team, vendors and sponsor effectively;

Qualifications

• Bachelors degree in a life sciences field;
• Maintain thorough knowledge of project and ability to coordinate/present at internal/external meetings and conference calls;
• Excellent computer (word-processing, databases, Excel, Windows) and organizational skills.

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.