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For Companies At a Glance
- Tasks: Manage clinical trials, ensuring compliance and overseeing project operations.
- Company: Medpace is a leading CRO dedicated to advancing medical therapeutics globally.
- Benefits: Enjoy flexible work options, competitive pay, and generous PTO.
- Why this job: Make a real impact on patients' lives while growing in a supportive environment.
- Qualifications: Bachelor's degree in health/life sciences; 5+ years of clinical trial management experience required.
- Other info: Remote work available for experienced candidates; join a recognised leader in the industry.
The predicted salary is between 43200 - 72000 £ per year.
Job Summary
Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Clinical Trial Managers with expertise in Nephrology are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. We provide remote flexibility only with relevant experience. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.
Responsibilities
- Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations.
- Serve as primary Sponsor contact for operational project-specific issues and study deliverables.
- Maintain in-depth knowledge of protocol, therapeutic area, and indication.
- Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided.
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable.
- Develop operational project plans.
- Manage risk assessment and execution.
- Responsible for management of study vendor.
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.
Qualifications
- Bachelor’s degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred.
- Experience in Phases 1-4; Phases 2-3 preferred.
- Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred.
- 5+ years of Project Manager/Clinical Trial Manager experience at a CRO required for a remote-based role.
- Management of overall project timeline.
- Bid defense experience preferred.
- Strong leadership skills.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace 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.
Awards
- Recognized by Forbes as one of America\’s Most Successful Midsize Companies in 2021, 2022, 2023, and 2024.
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
EO/AA Employer M/F/Disability/Vets
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Clinical Trial Manager (Nephrology) employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager (Nephrology)
✨Tip Number 1
Familiarise yourself with the latest trends and developments in nephrology. This will not only enhance your knowledge but also demonstrate your commitment to the field during interviews.
✨Tip Number 2
Network with professionals in the clinical trial management space, especially those with experience in nephrology. Attend relevant conferences or webinars to make connections that could lead to job opportunities.
✨Tip Number 3
Prepare to discuss your previous project management experiences in detail, particularly any that involved phases 1-4 of clinical trials. Be ready to highlight your leadership skills and how you've managed timelines and teams effectively.
✨Tip Number 4
Research Medpace thoroughly, including their recent projects and company culture. Tailoring your conversation to align with their mission and values can set you apart from other candidates.
We think you need these skills to ace Clinical Trial Manager (Nephrology)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trial management, particularly in nephrology. Emphasise your leadership skills and any specific projects you've managed that align with the responsibilities outlined in the job description.
Craft a Compelling Cover Letter: Write a cover letter that not only showcases your qualifications but also expresses your passion for clinical research and how you can contribute to Medpace's mission. Mention your familiarity with ICH/GCP guidelines and any experience with project timelines.
Highlight Relevant Experience: In your application, clearly outline your experience in Phases 1-4 of clinical trials, especially Phases 2-3. Include specific examples of your role in managing study vendors and ensuring site quality.
Showcase Your Soft Skills: Medpace values strong leadership and communication skills. In your application, provide examples of how you've successfully led teams or managed cross-functional projects, demonstrating your ability to handle operational project-specific issues.
How to prepare for a job interview at Medpace
✨Know Your Nephrology Stuff
Make sure you brush up on your knowledge of nephrology and related clinical trials. Be prepared to discuss specific studies or protocols you've worked on, as this will demonstrate your expertise and passion for the field.
✨Showcase Your Leadership Skills
As a Clinical Trial Manager, you'll need strong leadership abilities. Prepare examples of how you've successfully led teams, managed conflicts, or improved project outcomes in previous roles. This will help you stand out as a candidate.
✨Understand the Regulatory Landscape
Familiarise yourself with ICH/GCP guidelines and any relevant regulations. Being able to discuss how you've ensured compliance in past projects will show that you take these responsibilities seriously and can manage risk effectively.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and decision-making abilities. Think of scenarios where you've had to manage project timelines, vendor relationships, or site quality, and be ready to explain your approach and the outcomes.
