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

JR United Kingdom; London; Hybrid; GBP 60,000 - 100,000; Full time

Job summary

An established industry player seeks a Clinical Trial Manager with specialized expertise in Cardiovascular and Renal therapeutic areas. This role offers a unique opportunity to lead global clinical trials, leveraging your PhD in a hands-on capacity. You will manage complex studies from initiation to completion while ensuring alignment with therapeutic best practices and regulatory requirements. Join a growing CRO that focuses on cutting-edge studies in high-demand specialties, where your contributions will significantly impact patient outcomes. If you thrive in structured, onsite collaborative environments, this career-defining opportunity awaits you.

Qualifications

• 3+ years of hands-on clinical trial management in specialized therapeutic areas.
• Stable career progression with proven ability to manage multi-country trials.

Responsibilities

• Lead and execute global clinical trials for a top-tier CRO.
• Engage directly with sponsors as the scientific-operational interface.

Skills

Clinical Trial Management

Therapeutic Expertise in Cardiovascular

Operational Delivery

Cross-Functional Team Leadership

Regulatory Compliance

Education

PhD in Life Sciences or Medicine

Job description

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

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Client:

Location:

london, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

4

Posted:

05.05.2025

Expiry Date:

19.06.2025

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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