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:
* Line management of Clinical Research Associates (CRAs)
* Recruitment
* Involvement in training and development of the CRAs in collaboration with Training&Development department
* Oversight of CRAs to ensure they meet expectations
* Tracking and management of CRA Resourcing and allocation of studies assignment
* Turnover and retention of CRAs to meet company objectives
* Assist Clinical Trial Managers (CTM) with achieving project objectives in regards to CRA performance standards, monitoring consistency and compliance; also in trouble shooting and serve as a resource for issue resolution
* May serve as a lead CRA as needed
Qualifications:
* Life Science Bachelor's degree
* At least 4 years' experience as CRA in specified country
* Minimum 2-3 years of experience as CRAM
* Advanced knowledge of Good Clinical Practice and Local Regulations
* Strong leadership, mentoring, and motivational skills
* Effective written and verbal communication skills
* Proficient knowledge of Microsoft(r) Office software
* Fluent in English and Spanish
* This position is office based in Madrid, Spain
* Occasional travel (10-20%)
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