Clinical Trial Manager

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 contactJoe Footat 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.