Clinical Trial Manager (Oncology/Cardiovascular/Endocrine/Metabolic)

Medpace; Heverlee; Hybrid; EUR 85,000 - 125,000; Full time

Benefits offered by this job

Competitive compensation

Health and retirement benefits

WFH after training

Company-sponsored social events

Job summary

Medpace is seeking an experienced Clinical Trial Manager to join our Belgium-based team in Leuven. You will oversee day-to-day project operations across Phases 1-4, act as primary Sponsor contact, and ensure compliance with ICH/GCP and contractual requirements.

We welcome experts in Oncology/Cardiovascular/Endocrine/Metabolic who can either continue in their area or expand to new therapeutic areas; remote flexibility is available for candidates with relevant experience.

Qualifications

• Bachelor’s degree in health or life or life sciences; advanced degree preferred.
• 3+ years of Clinical Trial Management experience, CRO experience preferred.
• Experience in Phases 1-4; Phases 2-3 preferred.
• Strong leadership skills; ability to manage timelines; bid defense experience preferred.

Responsibilities

• Manage day-to-day operations of the project per contract and ICH/GCP requirements.
• Serve as primary Sponsor contact for operational issues and study deliverables.
• Maintain knowledge of protocol, therapeutic area, and indication.
• Provide cross-functional oversight and ensure necessary training.
• Review study protocol, edit checks, data analysis plan, and final report when applicable.
• Develop operational project plans and manage risk; oversee vendors.
• Manage site quality and supervise project CRAs and monitoring deliverables.

Skills

Trial management

Leadership

Bid defense

Phases 1-4 experience

Education

Bachelor’s degree 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 Belgium, Leuven. Clinical Trial Managers with expertise in Oncology/Cardiovascular/Endocrine/Metabolic are welcome to continue to work in their area of expertise or to expand to a new therapeutic area.We provide remote flexibility only with relevant experience. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.

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


• 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;


• Experience in Phases 1-4; Phases 2-3 preferred;


• Minimum of 3 years of Clinical Trial Management experience, CRO experience preferred;


• Management of overall project timeline;


• Bid defense experience preferred; and


• Strong leadership skills.

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

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

Collaborative Culture

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  • 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

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  • 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

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  • 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.