Clinical Trial Manager (Nephrology/Oncology/Cardiovascular/Endocrine/Metabolic)

JR United Kingdom; Slough; On-site; GBP 60,000 - 80,000; Full time

Job summary

A global CRO is seeking a Clinical Trial Manager specializing in Cardiovascular, Renal, or Gastrointestinal areas to lead complex global trials. Ideal candidates will possess a PhD, significant trial management experience, and strong operational delivery skills, making this position a career-defining opportunity.

Qualifications

• 3+ years of hands-on clinical trial management experience.
• Proven ability to manage multi-country trials.
• Stable career progression with less than 3 employers in the last 6 years.

Responsibilities

• Lead execution of global clinical trials in Cardiovascular, Renal or GI areas.
• Ensure trial execution aligns with best practices and regulatory requirements.
• Maintain 80% onsite presence with 20% remote flexibility.

Skills

Clinical trial management

Scientific expertise

Operational delivery

Education

PhD in Life Sciences or related discipline

Job description

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Clinical Trial Manager (Nephrology/Oncology/Cardiovascular/Endocrine/Metabolic), slough

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Client:

Location:

slough, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

4

Posted:

31.05.2025

Expiry Date:

15.07.2025

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Job Description:

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
• Must have worked at a global CRO
• Track record of managing multi-country trials with a focus on operational delivery
• Stable career progression (≤3 employers in last 6 years)
• Demonstrated promotions or increasing responsibility in clinical operations
• 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