Medpace/UK Virtual PhD Networking Event

US-OH-Cincinnati

US Careers

Req #: 11358
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 5,000 people across 40+ countries.

Responsibilities:

Below are the positions we will be recruiting for at this event: 

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

* Perform quality checks on submission documents and site essential documents
* Prepare and approve informed consent forms
* Serve as a Sponsor point of contact for start-up and regulatory submissions item

Associate Clinical Trial Manager

*  Management of project timeline and all project deliverables
* Responsible for leading internal project team members
* Postdoctoral Research or Healthcare research
experience required

Qualifications:

* Pursuing a PhD or completing Post Doctoral research in life science related field (GPA 3.5 and above);
* Stable work history;
* Able to work office-based in Cincinnati, OH
			
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