Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead clinical trials, manage project operations, and ensure compliance with regulations.
- Company: Medpace is a top CRO supporting biotech firms globally, focused on innovative medical solutions.
- Benefits: Enjoy flexible work options, competitive pay, generous PTO, and wellness initiatives.
- Why this job: Make a real impact on patients' lives while growing in a supportive, award-winning environment.
- Qualifications: Bachelor's degree in health sciences; 5+ years in clinical trial management required.
- Other info: Remote work available for experienced candidates; join a team recognised for excellence.
The predicted salary is between 48000 - 84000 £ per year.
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 Stirling, UK. Clinical Trial Managers with expertise in Oncology or other therapy areas 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; and 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 #J-18808-Ljbffr
Clinical Trial Manager (Associate Director) - Stirling employer: Medpace, Inc.
Contact Detail:
Medpace, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager (Associate Director) - Stirling
✨Tip Number 1
Network with professionals in the clinical trial management field, especially those who have experience at Medpace or similar CROs. Attend industry conferences or webinars to connect with potential colleagues and learn more about the company culture.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in clinical trials, particularly in oncology and other relevant therapeutic areas. This knowledge will not only boost your confidence but also demonstrate your commitment to staying updated in the field.
✨Tip Number 3
Prepare to discuss your previous project management experiences in detail, focusing on how you managed timelines, risks, and team dynamics. Be ready to provide specific examples that highlight your leadership skills and ability to handle complex projects.
✨Tip Number 4
Research Medpace's recent projects and achievements, especially in the oncology sector. Being knowledgeable about their work will help you tailor your conversation during interviews and show your genuine interest in joining their team.
We think you need these skills to ace Clinical Trial Manager (Associate Director) - Stirling
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trial management, especially in oncology or other therapeutic areas. Use specific examples to demonstrate your expertise and leadership skills.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for the role and the impact of clinical trials on patient lives. Mention why you want to work with Medpace specifically.
Highlight Relevant Experience: In your application, emphasise your experience in managing clinical trials, particularly Phases 1-4. Include any bid defense experience and your ability to manage project timelines effectively.
Showcase Your Knowledge: Demonstrate your understanding of ICH/GCP guidelines and the regulatory environment. Mention any specific training or certifications you have that are relevant to the role.
How to prepare for a job interview at Medpace, Inc.
✨Know Your Protocols
Familiarise yourself with the specific protocols and therapeutic areas relevant to the role. Being able to discuss these in detail will demonstrate your expertise and commitment to the position.
✨Showcase Leadership Skills
Prepare examples of how you've successfully led teams or managed projects in the past. Highlighting your leadership experience will be crucial, especially since the role requires strong oversight of internal project teams.
✨Understand Risk Management
Be ready to discuss your approach to risk assessment and management in clinical trials. This is a key responsibility for the role, so showcasing your knowledge and experience in this area will set you apart.
✨Ask Insightful Questions
Prepare thoughtful questions about Medpace's operations, culture, and future projects. This shows your genuine interest in the company and helps you assess if it's the right fit for you.
