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- Tasks: Lead global clinical trials and ensure operational success across high-impact studies.
- Company: Apsida Life Science partners with biotech and pharma for innovative clinical development.
- Benefits: Enjoy remote flexibility, competitive salary, equity schemes, and a structured career path.
- Why this job: Take ownership of impactful projects in a supportive culture focused on work-life balance.
- Qualifications: Bachelor’s degree in life sciences and 5+ years of Clinical Trial Management experience required.
- Other info: Opportunity to specialise in nephrology and related areas with a global reach.
The predicted salary is between 43200 - 72000 £ per year.
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:
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
Network with professionals in the clinical trial management field. Attend industry conferences, webinars, and local meetups to connect with others who work in CROs or related areas. Building these relationships can lead to valuable insights and potential job referrals.
✨Tip Number 2
Stay updated on the latest trends and regulations in clinical trials, especially in nephrology and other specialty areas. This knowledge will not only enhance your expertise but also demonstrate your commitment to the field during interviews.
✨Tip Number 3
Prepare for interviews by practising common questions specific to clinical trial management. Focus on scenarios that highlight your leadership skills and experience managing complex projects, as these are crucial for the role.
✨Tip Number 4
Research Apsida Life Science and their clients thoroughly. Understanding their values, mission, and the specific therapeutic areas they focus on will help you tailor your discussions and show genuine interest in the position.
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 protocol design and risk assessment.
Highlight Relevant Qualifications: Clearly state your educational background, especially if you have a Bachelor’s or advanced degree in life sciences. Emphasise your 5+ years of experience in clinical trial management and any specific achievements that relate to the role.
Showcase Soft Skills: In your application, highlight soft skills such as communication, teamwork, and problem-solving. These are crucial for the role, especially since you'll be acting as the main point of contact for sponsor stakeholders and overseeing internal project teams.
How to prepare for a job interview at Apsida Life Science
✨Know Your Therapeutic Area
Make sure to research and understand the specific therapeutic area related to the role, especially nephrology. Being able to discuss recent developments or challenges in this field will demonstrate your commitment and expertise.
✨Showcase Your Leadership Skills
Prepare examples of how you've successfully led clinical trials in the past. Highlight your ability to coordinate cross-functional teams and manage project timelines effectively, as these are crucial for the Clinical Trial Manager role.
✨Understand Regulatory Standards
Familiarise yourself with Good Clinical Practice (GCP) and other regulatory standards relevant to clinical trials. Be ready to discuss how you have ensured compliance in previous roles, as this is a key responsibility of the position.
✨Prepare for Scenario-Based Questions
Anticipate questions that may ask how you would handle specific challenges in clinical trial management, such as risk assessments or stakeholder communication. Practising your responses can help you articulate your thought process clearly during the interview.
