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Clinical Trial Manager (Nephrology)

3-5 years
Preferred by Comapny
11 Nov. 25, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Opportunity: Clinical Trial Manager (Nephrology)

Location: London, United Kingdom
Job Requisition ID: 10432
Time Type: Full-Time


About Medpace

Medpace is a leading global contract research organization (CRO) that specializes in Phase I-IV clinical development services for the biotechnology, pharmaceutical, and medical device industries. We are dedicated to accelerating the development of safe and effective medical therapeutics through our scientific and disciplined approach, with a presence in over 40 countries.


Role Overview

Medpace is expanding its Clinical Trial Management Group and is looking for Clinical Trial Managers (CTMs)with expertise in Nephrology to join our team in London, UK. This is an exciting opportunity for professionals looking to continue their career in Nephrology or expand into new therapeutic areas. Remote work flexibility is available for candidates with relevant experience.


Key Responsibilities

  • Project Management: Oversee day-to-day project operations in compliance with ICH/GCP guidelines and all applicable regulations.
  • Sponsor Interaction: Act as the primary contact for sponsors, addressing operational issues and ensuring study deliverables are met.
  • Therapeutic Knowledge: Maintain comprehensive knowledge of the study protocol, therapeutic area, and specific indications.
  • Cross-functional Team Oversight: Provide leadership and guidance to internal project teams, ensuring training and deliverables are completed.
  • Study Protocol Review: Contribute to the review and input for study protocols, edit check specifications, data analysis plans, and final reports.
  • Operational Planning: Develop and implement operational project plans, including risk management.
  • Vendor Management: Oversee the management of study vendors and ensure high-quality site management and deliverables.
  • Clinical Research Associate Supervision: Directly supervise project Clinical Research Associates (CRAs) and monitor site quality.

Qualifications

  • Education: Bachelor's degree in a health or life science-related field (Advanced degree preferred).
  • Experience:
    • Minimum of 5 years in Clinical Trial Management (CRO experience preferred).
    • Experience with Phases 1-4, with a preference for Phases 2-3.
    • At least 5 years of experience as a Project Manager/Clinical Trial Manager in a CRO, especially for remote roles.
  • Skills:
    • Strong leadership and project management capabilities.
    • Experience with Bid Defense is preferred.
    • Proven ability to manage timelines and ensure deliverables.

Why Medpace?

Perks & Benefits

  • Flexible work environment and competitive salary/bonus program.
  • Generous PTO packages and health/wellness initiatives.
  • Career growth opportunities and company-sponsored employee events.
  • Equity grants and structured career paths for professional development.

Recognition & Awards

  • Forbes: Named one of America’s Most Successful Midsize Companies (2021, 2022, 2023, 2024).
  • CRO Leadership Awards: Recognized for expertise, quality, and capabilities by Life Science Leader Magazine.

How to Apply

To join Medpace and make a meaningful contribution to Nephrology research, visit Medpace’s website and apply referencing Job Requisition ID 10432.


Join Medpace and help shape the future of clinical research. Apply now to make a difference!

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