Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.
Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective.
Headquartered in Cincinnati, Ohio, Medpace employs approximately 5,800 people across 43 countries.

Medpace

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medical-director

Medpace is a full-service contract research organization (CRO) that accelerates the development of safe and effective medical therapeutics. The company offers a comprehensive range of services to biopharmaceutical companies, including clinical trial management, regulatory affairs, and integrated laboratory services. With expertise across various therapeutic areas, Medpace facilitates collaboration among medical professionals to optimize the clinical development process and enhance trial efficiency.

Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 5,800 people across 43 countries.

• Manage and provide accountability for day-to-day project operations according to the contract, ICH/GCP, and applicable laws and regulations
• Serve as the primary Sponsor contact for operational project-specific issues and study deliverables
• Maintain in-depth knowledge of the protocol, therapeutic area, and indication
• Provide cross-functional oversight of internal project team members and deliverables
• Ensure necessary project-specific training is provided
• Review and provide input for study protocols, edit check specifications, data analysis plans, and final study reports when applicable
• Develop operational project plans
• Manage risk assessment and execution
• Manage study vendors where applicable
• Manage site quality and monitoring deliverables

Associate Director, Clinical Trial Management

Clinical trial management leader overseeing CRO project operations, sponsors, vendors, timelines, and deliverables. Supporting Medpace’s clinical development services for biotech, pharmaceutical, and medical device clients.

clinical-research

• Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP
• Maintain ongoing site correspondence and site files
• Complete visit reports and maintain study-related databases
• Provide oversight and interact with clinical research sites
• Review patient charts and clinical research data
• Participate in customized PACE training and onboarding
• Work with international teams of Clinical Research Associates
• Support clinical development projects across various therapeutic areas and nationwide site assignments

Bilingual Clinical Research Associate – Clinical Research Coordinator Experience

Home-based Clinical Research Associate conducting site visits and monitoring clinical trials for Medpace, a full-service CRO. Supporting biotechnology, pharmaceutical, and medical device development.

Medpace

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Associate Director, Clinical Trial Management

Medpace

Bilingual Clinical Research Associate – Clinical Research Coordinator Experience

Medpace