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For Companies At a Glance
- Tasks: Lead global clinical trials and ensure operational success across complex studies.
- Company: Join Apsida Life Science, a trusted recruitment partner in the biotech and pharmaceutical sectors.
- Benefits: Enjoy remote flexibility, competitive salary, equity schemes, and a structured career path.
- Why this job: Make a real impact in healthcare while working in a supportive and dynamic environment.
- Qualifications: Bachelor's degree in life sciences and 5+ years of Clinical Trial Management experience required.
- Other info: Opportunity to specialise in nephrology with a flexible hybrid work model.
The predicted salary is between 43200 - 72000 £ per year.
Job Description
Job Title:
Clinical Trial Manager
Location:
United States, Europe, United Kingdom, Australia, Asia (these are hybrid office based roles)
Salary:
Highly competitive
Contract Type:
Permanent
Apsida Life Science is currently partnering with a global, full-service CRO supporting biotech and pharmaceutical sponsors across all phases of clinical development. With a strong reputation in therapeutic leadership and global execution, this organisation is expanding as it continues to deliver high-quality trials in nephrology and other specialty areas.
This is an excellent opportunity for Clinical Trial Managers to take full ownership of global Phase I–IV trials while benefiting from a structured, supportive environment and long-term growth prospects. You’ll work cross-functionally and play a pivotal role in ensuring operational success across a portfolio of complex, high-impact studies.
Responsibilities:
- Lead day-to-day operations of assigned studies in accordance with protocol, GCP, and regulatory standards
- Act as the main point of contact for sponsor stakeholders on project deliverables and timelines
- Maintain deep knowledge of the therapeutic area and specific study protocols
- Oversee and support internal project team members including CRAs
- Contribute to protocol design, data analysis plans, and final study reports
- Develop and manage operational project plans, including timelines and vendor activities
- Conduct risk assessments and implement mitigation strategies across study components
- Ensure site monitoring quality and CRA performance through direct supervision
Qualifications:
- Bachelor’s degree in life sciences or related discipline (advanced degree preferred)
- 5+ years of Clinical Trial Management experience, ideally with CRO exposure
- Demonstrated experience across Phases 1–4 (Phases 2–3 preferred)
- Strong leadership and cross-functional coordination capabilities
- Experience managing full project timelines and site/vendor oversight
- Prior participation in bid defence processes is a plus
- Remote flexibility available for candidates with minimum 5 years' CRO-based CTM experience
Position Highlights:
- Global project ownership across Phases I–IV in a high-impact therapeutic area
- Remote flexibility for experienced candidates with a proven CRO background
- Lucrative equity scheme alongside competitive salary and bonus
- Structured career path within a high-performing and stable organisation
- Therapeutic depth: Opportunity to specialise or expand within nephrology and related areas
- Work-life balance: Flexible hybrid model and supportive company culture
If you are interested in learning more, please contact Joe Foot at Apsida Life Science: Joe.foot@apsida.com
Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) & Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost effective, high quality and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.
Clinical Trial Manager employer: Apsida Life Science
Contact Detail:
Apsida Life Science Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in clinical trials, especially in nephrology. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.
✨Tip Number 2
Network with professionals in the clinical trial management space, particularly those who have experience with CROs. Attend industry conferences or webinars to make connections that could lead to referrals or insider information about the role.
✨Tip Number 3
Prepare to discuss specific examples of how you've successfully managed complex studies in the past. Highlight your leadership skills and ability to coordinate cross-functional teams, as these are crucial for the Clinical Trial Manager position.
✨Tip Number 4
Research Apsida Life Science and their approach to clinical trials. Understanding their values and mission can help you tailor your conversations and show that you're genuinely interested in contributing to their success.
We think you need these skills to ace Clinical Trial Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trial management, especially your work with CROs and across Phases I-IV. Use specific examples to demonstrate your leadership and project management skills.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical trials and your understanding of the therapeutic areas mentioned in the job description. Mention how your background aligns with the responsibilities outlined, particularly your experience in managing complex studies.
Highlight Relevant Qualifications: Clearly state your educational background, especially if you have a degree in life sciences or an advanced degree. Include any certifications or training related to Good Clinical Practice (GCP) and regulatory standards.
Showcase Soft Skills: In your application, emphasise your soft skills such as communication, teamwork, and problem-solving abilities. These are crucial for the role, especially since you'll be acting as the main point of contact for sponsors and leading cross-functional teams.
How to prepare for a job interview at Apsida Life Science
✨Know Your Protocols
Familiarise yourself with the specific study protocols and GCP guidelines relevant to the role. Being able to discuss these in detail will demonstrate your expertise and commitment to compliance.
✨Showcase Leadership Skills
Prepare examples of how you've successfully led teams in previous clinical trials. Highlight your ability to coordinate cross-functionally and manage project timelines effectively.
✨Understand the Therapeutic Area
Research nephrology and any other specialty areas mentioned in the job description. Showing a deep understanding of the therapeutic landscape will set you apart from other candidates.
✨Prepare for Scenario Questions
Anticipate questions about risk assessments and mitigation strategies. Be ready to discuss how you've handled challenges in past projects, as this will showcase your problem-solving skills.
