Clinical Trial Manager

Precision Medicine Group; United Kingdom; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading precision medicine company is seeking a Clinical Trial Manager to oversee the management and operational delivery of clinical trials in the UK. This role requires strong leadership in clinical trial oversight, significant experience in oncology, and capability to manage remote teams across several countries. You will ensure high-quality standards and effective communication with stakeholders while driving the success of clinical trials. This position offers flexibility for remote work from the UK and other located countries.

Qualifications

• Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, pharma or biotech company.
• Significant clinical trial management experience in oncology.
• Working knowledge of GCP/ICH guidelines and the clinical development process.

Responsibilities

• Management of clinical trial elements including site selection and enrollment management.
• Ensure completion of trial deliverables.
• Mentoring and training of team members.
• Identify challenges to study timelines and offer creative action plans.

Skills

Computer skills (MS Office, MS Project, PowerPoint)

Software experience (CTMS, eTMF, EDC, IXRS)

Understanding of medical terminology

Knowledge of ICH-GCP

Education

Bachelor’s degree in a science or health-related field

Job description

Clinical Trial Manager

Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team. Candidates can work remotely in UK, Hungary, Poland, Romania, Serbia, or Slovakia.

Precision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry‑leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal passion for rare diseases and oncology, in addition to working across other therapeutic areas.

You will be the hub of central intelligence for the studies you manage, leading CRAs and overseeing all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high‑energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity.

We are addressing the challenges facing the R&D of novel compounds in oncology and are dedicated to positively impacting the health and lives of patients worldwide. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don’t miss exploring working with us.

About You

• You love having responsibility and a say in how clinical trials are run.
• You plan ahead but have alternative options and a flexible approach.
• You are client focused.
• You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.
• You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly.
• You are a master at identifying any risks that threaten projects and handle them resolutely.
• You thrive and work with autonomy and ownership to deliver successful outcomes.

Day‑to‑Day Role

• Management and operational delivery of the clinical elements within a trial including site selection, start‑up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning activities and close‑out.
• Successful execution of assigned trials and ensuring completion of trial deliverables.
• Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members.
• Mentoring and training of team members.
• Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor.
• Lead CRAs as they establish relationships with their sites for high‑quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities.
• Maintain team focus on study priorities through efficient cross‑functional partnerships and effective communication to achieve the highest level of client satisfaction.

Qualifications

• Bachelor’s degree or equivalent combination of education/experience in a science or health‑related field, including experience in oncology.

Other Required

• Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, pharma or biotech company (in a dedicated 'clinical lead' role).
• Significant clinical trial management experience in the area of oncology.
• Working knowledge of GCP/ICH guidelines and the clinical development process.
• Availability for domestic and international travel including overnight stays.
• Must be able to communicate effectively in English.

Skills

• Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS).
• Demonstrated ability to develop positive working relationships with internal and external organizations.
• Demonstrates core understanding of medical terminology and clinical trial activities as they relate to the execution of a clinical development plan.
• Demonstrates mastery knowledge of ICH‑GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement them.

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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [e-mail].