Medical Doctor / MBBS Career Event: Clinical Trial Management – Medpace London
Medpace, Inc. · GB
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About the Role
Medpace is seeking candidates with a Bachelor of Medicine, Bachelor of Surgery qualification for a full-time, office-based Associate Clinical Trial Manager role. This is an opportunity for Medical Doctors to transition into the Clinical Trials Industry, receiving foundational training and developing a career in therapeutic research and development.
Responsibilities
- Communicate and collaborate on global study activities, working closely with the project coordinator and clinical trial manager
- Ensure timely delivery of recurrent tasks with a high degree of accuracy
- Compile and maintain project-specific status reports within the clinical trial management system
- Interact with the internal project team, Sponsor, study sites, and third-party vendors
- Provide oversight and quality control of the internal regulatory filing system
- Provide oversight and management of study supplies
- Create and maintain project timelines
- Coordinate project meetings and produce quality minutes
Requirements
- Bachelor of Medicine, Bachelor of Surgery
- 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 not required but will be advantageous
Skills
- Analytical skills
- Academic skills
- Clinical project administration
- Clinical project management
- Presentation skills
Location
- Central London
Work Type
- Full-time
- Office-based
Experience Level
- Junior doctors
- Accelerated career path into Clinical Trial Management (CTM)
Education Level
- Bachelor of Medicine, Bachelor of Surgery
Benefits
- Competitive compensation programs
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events
About the Company
- Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research.
- We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective.
- Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.