Medical Trials Specialist

18 hours ago


London, Greater London, United Kingdom Medpace Full time
Job Overview:

Medpace is a leading full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.

Key Responsibilities:
  • Provide medical management and expertise for clinical trials;
  • Contribute medical expertise to study reports, regulatory documents, and manuscripts;
  • Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;
  • Participate in new business development through involvement in proposal and sponsor meetings as requested;
  • Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;
  • Follow specific research related protocol and lead others in strict adherence to the policies.
Requirements:
  • M.D., specialization in Oncology, and current medical licensure;
  • Board certification;
  • Prior clinical trial research experience preferred;
  • Previous experience in pharmaceutical-related clinical research is preferred.
Perks:
  • Flexible work environment;
  • Competitive compensation and benefits package;
  • Competitive PTO packages;
  • Structured career paths with opportunities for professional growth;
  • Company-sponsored employee appreciation events;
  • Employee health and wellness initiatives.

$130,000 - $150,000 per year.



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