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For Companies At a Glance
- Tasks: Lead clinical trial operations and ensure project success in a dynamic environment.
- Company: Medpace is a top CRO, driving innovation in biotech and improving patient lives globally.
- Benefits: Enjoy flexible work options, competitive pay, generous PTO, and wellness initiatives.
- Why this job: Make a real impact on healthcare while growing your career in a supportive culture.
- Qualifications: Bachelor's degree in health/life sciences; 5+ years in clinical trial management required.
- Other info: Remote work available for experienced candidates; join a recognised leader in the industry.
The predicted salary is between 48000 - 72000 £ 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.
- 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
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager (Associate Director) - Stirling
✨Tip Number 1
Familiarise yourself with Medpace's mission and values. Understanding their commitment to accelerating the development of medical therapeutics will help you align your responses during interviews, showcasing how your experience and passion fit into their goals.
✨Tip Number 2
Network with current or former employees of Medpace, especially those in clinical trial management roles. They can provide valuable insights into the company culture and expectations, which can give you an edge in discussions.
✨Tip Number 3
Highlight your experience in managing clinical trials, particularly in oncology or other relevant therapeutic areas. Be prepared to discuss specific projects you've led, focusing on your leadership skills and ability to manage timelines and deliverables.
✨Tip Number 4
Prepare for questions about risk assessment and vendor management, as these are crucial aspects of the role. Think of examples from your past work where you successfully navigated challenges in these areas, demonstrating your problem-solving abilities.
We think you need these skills to ace Clinical Trial Manager (Associate Director) - Stirling
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the Clinical Trial Manager position. Understand the responsibilities and qualifications required, especially the emphasis on experience in Phases 1-4 and oncology.
Tailor Your CV: Customise your CV to highlight relevant experience in clinical trial management, particularly in oncology or other therapeutic areas. Emphasise your leadership skills and any specific project management achievements that align with the role.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for clinical research and how you can contribute to Medpace's mission. Mention any specific experiences that relate to the responsibilities listed in the job description.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects attention to detail, which is crucial in clinical trial management.
How to prepare for a job interview at Medpace
✨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 in previous roles. Highlight your ability to manage cross-functional teams and ensure project deliverables are met, as this is crucial for a Clinical Trial Manager.
✨Understand Risk Management
Be ready to discuss your experience with risk assessment and management in clinical trials. Providing concrete examples of how you've navigated challenges will show your problem-solving skills and strategic thinking.
✨Ask Insightful Questions
Prepare thoughtful questions about Medpace's projects, culture, and future directions. This not only shows your interest in the company but also helps you assess if it's the right fit for you.
