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:
* Provide comprehensive assessment of clinical trial study participants;
* Review assigned protocols for scientific and subject safety matters;
* Attend pre-study and study-related meetings with project teams;
* Assist the Clinical Operations team with clinical activities related to study participant recruitment, screening, study conduct and regulatory adherence;
* Assist with ensuring safety and protection of study subjects according to Good Clinical Practices, SOPs, ICH Guidelines, etc.; and
* Assist with protocol training of the study staff as needed.
Qualifications:
* Master's Degree and graduation from a Nurse Practitioner or Physician Aisstant Program;
* Three years of advanced nursing experience; and
* Current valid RN license in the state of Ohio.
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