Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead global clinical trials in Cardiovascular, Renal, or Gastrointestinal areas.
- Company: Join a top-tier global CRO known for its elite therapeutic focus.
- Benefits: Enjoy 20% remote work flexibility and a dynamic team environment.
- Why this job: Make an impact with your PhD while working on cutting-edge studies.
- Qualifications: PhD in Life Sciences or related field; 3+ years in clinical trial management.
- Other info: Ideal for Senior CTMs/CPMs focused on structured, onsite collaboration.
The predicted salary is between 48000 - 72000 £ per year.
Apsida has partnered with a global CRO currently seeking an accomplished Clinical Trial Manager with specialized expertise in Cardiovascular, Renal, or Gastrointestinal therapeutic areas to lead and execute global clinical trials for a top-tier CRO. This role demands a rare combination of deep therapeutic knowledge, operational excellence, and advanced scientific credentials to drive complex studies from initiation to completion.
Key Selection Criteria:
- Scientific & Therapeutic Expertise: Life Sciences, Medicine, or related discipline (ideally a PhD)
- 3+ years of hands-on clinical trial management exclusively in Cardiovascular, Renal, or GI/Gastrointestinal trials
- Proven ability to interpret and apply therapeutic insights to trial execution
- CRO Leadership Experience: Must have worked at a global CRO
- Track record of managing multi-country trials with a focus on operational delivery
- Career Profile: Stable career progression (≤3 employers in last 6 years)
- Demonstrated promotions or increasing responsibility in clinical operations
Role Expectations:
- Lead cross-functional study teams as the primary operational decision-maker
- Ensure trial execution aligns with therapeutic best practices and regulatory requirements
- Maintain 80% onsite presence (4 days/week) with 20% remote flexibility
- Directly engage with sponsors as the scientific-operational interface
Why This Role Stands Out:
- Elite therapeutic focus - Work on cutting-edge studies in high-demand specialties
- PhD utilization - Apply your advanced training in a hands-on, impactful capacity
- Career-defining opportunity - Join a growing CRO with unparalleled specialization
Application Process:
- Qualified candidates should submit:
- CV highlighting therapeutic-specific trial experience
- PhD certification
- Summary of CRO experience (including employer names/duration)
Note: Only candidates meeting all specified criteria will be considered. This specification targets: Senior CTMs/CPMs seeking to leverage their PhD in an operational leadership role. Professionals with unwavering focus on Cardiovascular/Renal/GI trials. Candidates who thrive in structured, onsite collaborative environments.
Clinical Trial Manager (Nephrology/Oncology/Cardiovascular/Endocrine/Metabolic) 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 (Nephrology/Oncology/Cardiovascular/Endocrine/Metabolic)
✨Tip Number 1
Network with professionals in the clinical trial management field, especially those who have experience in Cardiovascular, Renal, or Gastrointestinal trials. Attend industry conferences and seminars to connect with potential colleagues and learn about the latest trends in these therapeutic areas.
✨Tip Number 2
Familiarise yourself with the specific regulatory requirements and best practices for conducting clinical trials in your area of expertise. This knowledge will not only enhance your credibility but also demonstrate your commitment to operational excellence during interviews.
✨Tip Number 3
Prepare to discuss your previous experiences managing multi-country trials in detail. Highlight any challenges you faced and how you overcame them, as this will showcase your problem-solving skills and ability to lead cross-functional teams effectively.
✨Tip Number 4
Research the specific CRO you are applying to and understand their focus areas and recent projects. Tailoring your conversation to align with their goals and demonstrating your enthusiasm for their work can set you apart from other candidates.
We think you need these skills to ace Clinical Trial Manager (Nephrology/Oncology/Cardiovascular/Endocrine/Metabolic)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your specific experience in Cardiovascular, Renal, or Gastrointestinal trials. Emphasise any relevant roles and responsibilities that demonstrate your expertise in these therapeutic areas.
Showcase Your PhD: Include your PhD certification prominently in your application. Explain how your advanced training has equipped you with the skills necessary for leading clinical trials and making operational decisions.
Detail Your CRO Experience: Provide a summary of your experience working at a global CRO. Include employer names, duration of employment, and specific achievements in managing multi-country trials to showcase your leadership capabilities.
Highlight Onsite Collaboration Skills: Since the role requires an 80% onsite presence, emphasise your ability to thrive in structured, collaborative environments. Mention any previous experiences where you successfully led cross-functional teams in person.
How to prepare for a job interview at Apsida Life Science
✨Showcase Your Therapeutic Expertise
Make sure to highlight your specific experience in Cardiovascular, Renal, or Gastrointestinal trials. Be prepared to discuss how your knowledge has influenced trial execution and decision-making in previous roles.
✨Demonstrate Leadership Experience
Since the role requires CRO leadership experience, share examples of how you've successfully managed multi-country trials. Discuss your approach to leading cross-functional teams and ensuring operational delivery.
✨Prepare for Regulatory Discussions
Familiarise yourself with the regulatory requirements relevant to clinical trials in your therapeutic area. Be ready to explain how you ensure compliance and best practices during trial execution.
✨Emphasise Onsite Collaboration Skills
Given the role's requirement for an 80% onsite presence, convey your ability to thrive in structured, collaborative environments. Share experiences where your onsite engagement led to successful outcomes in trials.
