Entry Level Life Sciences Hiring Event - July 1st

BE-Leuven

International Careers

Req #: 12804
Type: Full-Time
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Medpace, Inc.

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				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 6,000 people across 40+ countries.

Responsibilities:

Below are some examples of the positions that we will discuss during the event.

Clinical Data Coordinator: 

* Validate entry database designs
* Report metrics and data trends on projects
* Identify data conflicts and issues on projects
* Work with personnel from global research sites to resolve data conflicts

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

Project Coordinator - CRO

* Partner with Clinical Trial Manager to coordinate daily study activities
* Central point of contact for internal and external team members
* Create and maintain project timeline

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

Medical technologist - MRL

* Perform documentation, and routine lab system operations.
* 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.
* Train on different sets of automated instrumentation to learn maintenance and troubleshooting skills.

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Qualifications:

* Bachelor's in Life Sciences or related fields
* Willing to work office-based in Leuven
			
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