Job Summary :
Medpace will be hosting a virtual info session targeting Bachelor's and Master's students in life sciences.
WHEN: September 15th at 11:00 AM
A first pre-screening will be done and if you're selected you will receive a MS Teams invite to follow the online event.
Responsibilities :
Below are some examples of the positions that we will discuss during the event.
Clinical Data Coordinator:
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Validate entry database designs
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Report metrics and data trends on projects
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Identify data conflicts and issues on projects
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Work with personnel from global research sites to resolve data conflicts
Clinical Research Associate
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Comprehensive training program that provides resources and knowledge to monitor sites independently
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Travel to non-local, national study sites 60-80% of the time
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Communicate with medical staff and clinical research physicians on site
Project Coordinator - CRO
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Partner with Clinical Trial Manager to coordinate daily study activities
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Central point of contact for internal and external team members
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Create and maintain project timeline
Medical technologist - MRL
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Perform documentation, and routine lab system operations.
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Problem solve and work alongside our team of Medical Laboratory Scientists and PhD Scientists to develop and validate new tests and methods for routine and biomarker testing in our expanding laborator.
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Train on different sets of automated instrumentation to learn maintenance and troubleshooting skills.
Qualifications :
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Bachelor's/ Master's in Life Sciences or related fields
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Willing to work office-based in Leuven
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.
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Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
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Office based environment with on-site mentors
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Defined career paths with clear advancement opportunities
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Industry renowned onboarding and training programs designed to accelerate professional development
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Ongoing training and continuous learning opportunities throughout your career
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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
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Comprehensive health, wellness, retirement, and PTO benefits
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Office based culture with occasional WFH that provides flexibility for eligible positions after training
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Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
