Job Title:
Associate Clinical Trial Manager (aCTM) We are seeking a highly motivated and experienced Associate Clinical Trial Manager to join our London Clinical Trial Management team. The successful candidate will have a strong background in Cardiovascular related research, excellent analytical and academic skills, and the ability to apply these skills in a clinical project administration and management role. The ideal candidate will have a PhD or Post-Doctoral Research experience in Life Sciences and fluency in English with solid presentation skills. They will be able to work effectively in a fast-paced dynamic industry within an international team and possess prior experience within the CRO or pharmaceutical industry (although not required). Responsibilities: Communicate and collaborate on global study activities Compile and maintain project-specific status reports within the clinical trial management system Interact with internal project teams, Sponsors, study sites, and third-party vendors Provide oversight and quality control of internal regulatory filing systems Create and maintain project timelines Coordinate project meetings and produce quality minutes Qualifications: PhD in Life Sciences Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry is advantageous but not required About Medpace: Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. 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. Why Choose Medpace? We offer a competitive compensation and benefits package, flexible work environment, and opportunities for professional growth. Our company-sponsored employee appreciation events and employee health and wellness initiatives make us a great place to work. As a recognized leader in the CRO industry, we continually receive awards for excellence in service, quality, and capabilities. Estimated Salary Range:
$60,000 - $80,000 per year
Associate Clinical Trial Manager (aCTM) We are seeking a highly motivated and experienced Associate Clinical Trial Manager to join our London Clinical Trial Management team. The successful candidate will have a strong background in Cardiovascular related research, excellent analytical and academic skills, and the ability to apply these skills in a clinical project administration and management role. The ideal candidate will have a PhD or Post-Doctoral Research experience in Life Sciences and fluency in English with solid presentation skills. They will be able to work effectively in a fast-paced dynamic industry within an international team and possess prior experience within the CRO or pharmaceutical industry (although not required). Responsibilities: Communicate and collaborate on global study activities Compile and maintain project-specific status reports within the clinical trial management system Interact with internal project teams, Sponsors, study sites, and third-party vendors Provide oversight and quality control of internal regulatory filing systems Create and maintain project timelines Coordinate project meetings and produce quality minutes Qualifications: PhD in Life Sciences Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry is advantageous but not required About Medpace: Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. 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. Why Choose Medpace? We offer a competitive compensation and benefits package, flexible work environment, and opportunities for professional growth. Our company-sponsored employee appreciation events and employee health and wellness initiatives make us a great place to work. As a recognized leader in the CRO industry, we continually receive awards for excellence in service, quality, and capabilities. Estimated Salary Range:
$60,000 - $80,000 per year
