Clinical Trial Manager (Nephrology)

3+ years

Preferred by Comapny

Leuven

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: Leuven, Belgium
Job Requisition ID: 10434
Time Type: Full-Time

About Medpace

Medpace is a leading global contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. We are headquartered in Cincinnati, Ohio, and operate in 40+ countries, dedicated to accelerating the development of safe and effective medical therapeutics.

Role Overview

Medpace is seeking Clinical Trial Managers (CTMs) with expertise in Nephrology to join our Clinical Trial Management Group in Leuven, Belgium. If you have experience in clinical trial management and want to contribute to global studies, especially in Nephrology, this is an excellent opportunity to grow your career. We also offer remote work flexibility for candidates with relevant experience.

Key Responsibilities

Project Operations Management: Ensure day-to-day operations of the clinical trial are executed as per contract, ICH/GCP guidelines, and other applicable regulations.
Sponsor Interaction: Serve as the primary contact for sponsors regarding operational project issues and deliverables.
Knowledge Management: Maintain in-depth knowledge of study protocol, therapeutic areas, and indications.
Cross-functional Team Oversight: Provide oversight to internal project team members, ensuring proper project-specific training and collaboration.
Document Review: Review and provide input for study protocols, data analysis plans, and final study reports.
Operational Planning: Develop and execute operational project plans, including risk assessments.
Vendor Management: Oversee study vendors and ensure compliance with quality standards.
Site Management: Manage site quality and supervise Clinical Research Associates (CRAs) to ensure timely 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).
- Phases 1-4 experience, with Phases 2-3 being highly preferred.
- 5+ years of experience in Project Management/Clinical Trial Management at a CRO, required for remote-based roles.
Skills:
- Strong leadership and project management skills.
- Experience in bid defense and project timeline management.

Why Medpace?

Perks & Benefits

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

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 make a global impact, visit Medpace’s website and submit your application referencing Job Requisition ID 10434.

Make a difference in clinical research with Medpace and contribute to advancing Nephrology studies and therapies. Apply today!

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Clinical Trial Manager (Nephrology)

Job Description

Job Opportunity: Clinical Trial Manager (Nephrology)

About Medpace

Role Overview

Key Responsibilities

Qualifications

Why Medpace?

Perks & Benefits

Recognition & Awards

How to Apply

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