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Clinical Trial Manager - Clinical Trial Services

Precision For Medicine
Precision For Medicine
0-2 years
Not Disclosed
10 Jan. 6, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Trial Manager – Clinical Trial Services (Remote, United Kingdom / Europe)

Location: Remote – United Kingdom (candidates may also be based in Hungary, Poland, Romania, Serbia, or Slovakia)
Job Type: Full-Time
Division: Precision for Medicine
Business Unit: Clinical Solutions
Requisition Number: 6273


About Precision for Medicine

Precision for Medicine is a precision medicine-focused Contract Research Organization (CRO) dedicated to accelerating the development of life-changing therapies. By integrating advanced clinical trial designs, biomarker and data analytics, operational expertise, and scientific insight, we enable faster, cost-effective, and high-quality delivery of clinical studies in oncology, rare diseases, and other therapeutic areas.

Our mission is to improve patient outcomes globally by supporting clinical research that is precise, efficient, and impactful. We value professionals who take ownership, embrace challenges, and contribute to trial success while fostering collaboration and continuous improvement.


Role Overview

We are seeking an experienced Clinical Trial Manager (CTM) to join our growing Clinical Trial Services team. This role is fully remote and involves leading cross-functional teams and CRAs, overseeing the operational and clinical execution of trials across multiple countries. You will ensure trials meet timelines, quality standards, and regulatory requirements, while mentoring team members and providing strategic insights to optimize study delivery.

This is a high-impact role for candidates with significant oncology clinical trial management experience, who thrive in dynamic, multi-country project environments.


Key Responsibilities

  • Lead and manage clinical trial operations, including site selection, study start-up, enrollment management, site engagement, monitoring, data cleaning, and trial close-out.

  • Ensure successful execution of clinical studies and completion of all trial deliverables on time and within scope.

  • Act as the central point of communication for cross-functional teams, sponsors, and investigators to maintain study oversight and alignment.

  • Mentor, train, and guide CRAs and other team members, ensuring high-quality monitoring and site support.

  • Identify risks to study timelines or quality and implement effective mitigation strategies.

  • Maintain adherence to GCP/ICH guidelines, regulatory requirements, and Precision SOPs.

  • Foster collaboration across internal and external stakeholders to achieve optimal client satisfaction.

  • Demonstrate a consultative approach to trial management, providing expert input to improve operational efficiency and decision-making.


Required Qualifications

  • Bachelor’s degree or equivalent in life sciences, health, or related fields; advanced degree preferred.

  • Significant clinical trial management experience in oncology, ideally in a CRO, pharmaceutical, or biotech environment.

  • Proven ability to lead multi-country clinical studies with responsibility for clinical and operational outcomes.

  • Strong knowledge of GCP/ICH guidelines, clinical development processes, and trial execution.

  • Effective written and verbal communication skills in English.

  • Availability for domestic and international travel, including overnight stays.


Preferred Skills & Competencies

  • Proficiency with clinical trial systems: CTMS, eTMF, EDC, IXRS, and MS Office (Word, Excel, PowerPoint, MS Project).

  • Strong organizational and project management skills with the ability to manage multiple priorities.

  • Demonstrated expertise in medical terminology, clinical trial operations, and oncology study execution.

  • Ability to develop and maintain positive working relationships with internal teams, sites, and sponsors.

  • Mastery of regulatory guidance and Precision SOPs with the ability to implement them effectively.


Why Join Precision for Medicine?

  • Lead cutting-edge oncology and precision medicine trials with global impact.

  • Take ownership of multi-country studies and influence trial outcomes.

  • Collaborate with experienced clinical teams in a supportive, remote-friendly environment.

  • Contribute to the development of therapies that transform patient care.


Application Notes

Applicants should remain cautious of fraudulent recruitment offers. All official communications and job offers will be issued only by Precision for Medicine’s recruiting team following a formal interview process.