Clinical Trial Job at Medpace, UK
Are you a junior doctor looking to enter clinical research in London? This Associate Clinical Trial Manager role at Medpace is an excellent opportunity for MBBS graduates. This Clinical Trial Job at Medpace Careers allows you to transition from clinical practice into the research and development sector. You will gain hands-on experience in clinical trial management and project coordination. The role offers structured training and career growth in a global environment. This Job in the UK is ideal for those aiming for a long-term career in clinical trials.
About Medpace:
Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, the company operates in more than 40 countries and employs more than 5,000 people.
Medpace focuses on accelerating the global development of safe and effective therapeutics through a scientific and disciplined approach. The organization has expertise across multiple therapeutic areas, including oncology, cardiology, metabolic diseases, and infectious diseases.
Recognized by Forbes as one of America’s Most Successful Midsize Companies from 2021 to 2024, Medpace is known for its quality, reliability, and innovation in clinical research.
Job Details:
- Job Title: Associate Clinical Trial Manager (aCTM)
- Location: London, United Kingdom
- Job Type: Full-Time
- Work Mode: Office-based
- Department: Clinical Trial Management
- Job ID: 12681
- Experience Required: Freshers / Junior Doctors
Key Responsibilities:
- Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
- Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
- Compile and maintain project-specific status reports within the clinical trial management system in this Clinical Trial Job at Medpace Careers
- Interact with the internal project team, Sponsor, study sites, and third-party vendors
- Provide oversight and quality control of our internal regulatory filing system
- Provide oversight and management of study supplies in this Job in the UK
- Create and maintain project timelines
- Coordinate project meetings and produce quality minutes
Educational Requirements for this Job:
- 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 Required:
- Strong analytical and organizational skills
- Excellent communication and interpersonal abilities
- Ability to work in a fast-paced and dynamic environment
- Attention to detail and accuracy
- Team collaboration and coordination skills
- Time management and multitasking abilities
- Willingness to learn and adapt in clinical research
Benefits of the Clinical Trial Job:
- Structured training and career development programs
- Opportunity to transition into clinical research
- International work environment exposure
- Competitive salary and benefits package
- Flexible work environment
- Paid time off (PTO) benefits
- Employee wellness initiatives
- Recognition and career growth opportunities
- Opportunity to work on cutting-edge therapeutics
