Clinical Project Coordinator - Entry

Medpace; Singapore; On-site; SGD 60,000 - 80,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation and benefits package

Structured career paths

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Job summary

A clinical research organization is seeking a Clinical Project Coordinator - Entry in Singapore. The role involves managing clinical trials, compiling project status reports, and supporting the clinical trial manager. Candidates should hold a bachelor's degree in a health sciences field and possess strong organizational and computer skills. This full-time position promises career growth and a flexible work environment, contributing to impactful clinical research.

Qualifications

• Maintain thorough knowledge of projects and coordinate/present at meetings.
• Ability to engage effectively with cross-functional teams and vendors.

Responsibilities

• Manage clinical trial on a day-to-day basis.
• Compile and maintain project-specific status reports.
• Support the clinical trial manager in drafting study plans.

Skills

Excellent computer skills (word-processing, databases, Excel, Windows)

Organizational skills

Education

Bachelor's degree in a health sciences field

Job description

Join to apply for the Clinical Project Coordinator - Entry role at Medpace

We are currently seeking a full-time, office-based Clinical Research Project Coordinator Entry to join our Clinical Trial Management team in Singapore. 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, enrollment projections etc.
• Update eTMF and perform ongoing eTMF QC.
• Support clinical trial manager to draft study plans and study specific guidance documents.
• Manage site feasibility, site activation preparation and study supply management.
• Communicate with regional cross-functional team, vendors and sponsor effectively.

Qualifications

• Bachelor's degree in a health 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.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I–IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What To Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Seniority level

Not Applicable

Employment type

Full‑time

Job function

Project Management and Information Technology

Industries

Pharmaceutical Manufacturing

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