Training Data

2 weeks ago


London, United Kingdom Medpace, Inc. Full time

By working cross functionally with our clinical operations, medical and regulatory submissions teams, researching internal and public domain databases, as well as through obtaining direct feedback from investigative sites, this individual will provide strategic insights on country selection and enrollment planning for global clinical trials. If you are an individual with a clinical background and expertise in clinical research, please review the following career opportunity. Entry-level positions are also available for new graduates.
Coordinate feasibility assessments and deliver high quality, accurate feasibility data to internal and external teams;
Perform outreach to investigative sites to obtain indication and protocol specific feedback;
Assist project teams with preparation for bid defense meetings; Bachelors degree in life sciences required, Masters or PhD preferred;
Ability to prioritize multiple projects and tasks within tight timelines;
Fluency in English language;
Working knowledge of feasibility processes and databases is highly desirable.
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.
When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.
In 2020, Medpace opened a new seven story building that is approximately 250,000 SQFT. The company also has expanding office locations in Dallas, TX and Denver, CO.
Company-sponsored social and wellness events
Hybrid work-from-home options and flexible work schedule
Free and covered parking
Discounts for local businesses
Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
EO/AA Employer M/F/Disability/Vets
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