Clinical Trial Manager (Nephrology)

3-5 years

Preferred by Comapny

Lyon

12 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: Lyon, France
Job Requisition ID: 10433
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. Headquartered in Cincinnati, Ohio, with a global presence in 40+ countries, we are committed to accelerating the development of safe and effective medical therapeutics.

Role Overview

Medpace is expanding its Clinical Trial Management Group and is seeking Clinical Trial Managers (CTMs) with expertise in Nephrology to join our team in Lyon, France. This role is ideal for professionals looking to continue their career in Nephrology or explore new therapeutic areas. Remote work flexibility is available for candidates with relevant experience.

Key Responsibilities

Project Operations Management: Oversee day-to-day project operations, ensuring compliance with ICH/GCP guidelines and other applicable regulations.
Sponsor Interaction: Serve as the main point of contact for sponsors, handling operational project issues and ensuring study deliverables are met.
Study Protocol and Knowledge: Maintain a thorough understanding of study protocols, therapeutic areas, and indications.
Cross-functional Team Oversight: Manage internal project team members and ensure all project-specific training and deliverables are executed.
Document Review: Review and contribute to study protocols, data analysis plans, and final reports.
Project Planning: Develop and manage operational project plans, including risk assessment and execution.
Vendor Management: Manage study vendors and ensure quality control throughout the project.
Site Management: Supervise Clinical Research Associates (CRAs) and manage site quality and deliverables.

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 in Project Management/Clinical Trial Management at a CRO, especially for remote roles.
Skills:
- Strong leadership and project management skills.
- Bid defense experience is preferred.
- Proven ability to manage project timelines and deliverables.

Why Medpace?

Perks & Benefits

Flexible work environment and competitive compensation.
Generous PTO and health/wellness initiatives.
Structured career development and growth opportunities.
Company-sponsored employee appreciation events.

Recognition & Awards

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

How to Apply

To join Medpace and contribute to advancing Nephrology studies, visit Medpace’s website and submit your application referencing Job Requisition ID 10433.

Make an impact in clinical research with Medpace. Apply today to help improve global healthcare!

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