Clinical Trial Manager (Oncology)

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

Job summary

An established industry player is seeking a Clinical Trial Manager to lead global clinical research studies in a dynamic office environment. In this pivotal role, you will manage timelines, coordinate services, and lead a cross-functional team to ensure successful execution of clinical trials. This position offers a unique opportunity to contribute to groundbreaking medical research while working closely with sponsors and supporting business development initiatives. Join a forward-thinking organization that values people, purpose, and passion, and make a significant impact in the field of clinical research.

Benefits

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Qualifications

• At least 2 years of clinical trial management experience in Asia Pacific.
• Experience in Oncology studies is required.

Responsibilities

• Lead global clinical trials and manage project deliverables.
• Coordinate all services contracted for the study.

Skills

Clinical Trial Management

Oncology Studies

Communication Skills

Project Management

Regulatory Knowledge

Education

Bachelor’s degree in a health related field

Master’s degree or PhD

Job description

Job Summary

Medpace is currently looking for Clinical Trial Manager (CTM) to lead global clinical research studies. This position is fully office-based in our Singapore office. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials.

Responsibilities

The Clinical Trial Manager position performs project lead role for multiservice global clinical trials. The position interacts with sponsors and manages the timeline and project deliverables. This role coordinates for all services contracted for the study. CTMs are also responsible for leading cross functional team of clinical monitoring, study start-up, regulatory, contract, safety, medical monitoring etc. CTM may need to attend bid defense meetings and support business development team in winning new business.

Qualifications

• Bachelor’s degree in a health related field (Master’s degree or PhD is preferred);
• At least two years of clinical trial management experience in Asia Pacific region ideally in a CRO environment;
• Experience in Oncology studies required;
• Excellent communication skills including good written and spoken English; and
• Flexible, accountable and comfortable in working in a global environment.

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.

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.

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