Clinical Trial Manager (Oncology)

Medpace, Inc.; Singapore; On-site; SGD 120,000 - 180,000; Full time

Benefits offered by this job

Competitive compensation

Health, wellness, retirement, PTO

WFH flexibility after training

Company-sponsored social events

Job summary

Medpace is seeking a Clinical Trial Manager to oversee day-to-day project operations within our Singapore group. You will serve as the Sponsor contact for operational issues and ensure study deliverables meet ICH/GCP guidelines while coordinating cross-functional teams.

The role requires oncology trial experience, strong English communication, and a flexible, globally oriented mindset. This is an on-site position based in Singapore within a leading CRO environment.

Qualifications

• Bachelor's degree in a health or life science-related field; advanced degree preferred.
• At least two years of clinical trial management experience in Asia Pacific, ideally in a CRO.
• Experience in Oncology studies is required.
• Excellent communication skills in written and spoken English.
• Flexible, accountable and comfortable working in a global environment.

Responsibilities

• Manage day-to-day operations of the project per contract and ICH/GCP guidelines.
• Serve as primary Sponsor contact for operational issues and study deliverables.
• Maintain in-depth knowledge of protocol, therapeutic area, and indication.
• Provide cross-functional oversight of internal project team members and training.
• Review and input for study protocol, edit check specs, data analysis plan, and final study report.

Skills

Communication skills

Oncology experience

Global/workplace flexibility

English proficiency

Accountability

Education

Bachelors in health or life sciences

Advanced degree in health or life sciences

Job description

Job Summary

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Singapore. Clinical Trial Managers with expertise in Oncology are welcome to continue to work in their area of expertise or to expand to a new therapeutic area.

Responsibilities

• Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations;
• Serve as primary Sponsor contact for operational project-specific issues and study deliverables;
• Maintain in depth knowledge of protocol, therapeutic area, and indication;
• Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided;
• Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable;
• Develop operational project plans;
• Manage risk assessment and execution;
• Responsible for management of study vendor; and
• Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.

Qualifications

• Bachelor’s degree in a health or life science-related field; Advanced degree in a health or life science-related field 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) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
• Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• Office based environment with on-site mentors
• Defined career paths with clear advancement opportunities
• Industry renowned onboarding and training programs designed to accelerate professional development
• Ongoing training and continuous learning opportunities throughout your career
• An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• Competitive compensation programs that recognize and reward performance
• Comprehensive health, wellness, retirement, and PTO benefits
• Office based culture with occasional WFH that provides flexibility for eligible positions after training
• Company-sponsored social events

Please note benefits may vary based on country.