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PhD Virtual Info Session – Medpace Belgium

Role overview

Qualifications

  • PhD in Life Sciences
  • Fluency in English with solid presentation skills
  • Ability to work in a fast-paced dynamic industry within an international team
  • Willing to work office-based in Leuven

Responsibilities

  • Communicate and coordinate study activities between the internal project team, Sponsor, study sites, third-party vendors.
  • Provide oversight and management of study supplies.
  • Conduct comprehensive training to monitor sites independently.
  • Communicate with research sites to collect essential documents for clinical trials.

Key facts

  • Remote from: Belgium
  • Full time
  • English

Other skills

  • Collaboration
  • Communication
  • Presentations
  • Teamwork
  • Problem Solving

About the company

Medpace logo

Medpace

Contract Research Organizations (CRO)

Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 5,800 people across 43 countries.

Company details

Company typeLarge
IndustryContract Research Organizations (CRO)
Company size5001 - 10000

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Job description

Job Summary :

Medpace will be hosting an Online Hiring Event targeting PhD's students in life sciences. 

 

WHEN: September 22 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.

     

     Associate Clinical Trial Manager: 

    • Communicate and coordinate study activities bewteen the internal project team, Sponsor, study sites, third-party vendors, working closely with the Project Coordinators and CTMs.
    • Provide oversight and management of study supplies.

    Clinical Research Associate 

    • Comprehensive training program that provides resources and knowledge to monitor sites independently
    • Travel to non-local, national study sites 60-80% of the time
    • Communicate with medical staff and clinical research physicians on site

    Regulatory Submissions Coordinator

    • Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial;
    • Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);
    • Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards
    •  

 

Qualifications :
  • PhD in Life Sciences
  • Fluency in English with solid presentation skills
  • Ability to work in a fast-paced dynamic industry within an international team
  • 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

    • 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. 

 

iCIMS_Job-Post-Banner_4

 

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.

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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