Clinical Project Manager / Senior Clinical Project Manager New Remote, United Kingdom

Precisionscientia; United Kingdom; Remote; GBP 50,000 - 75,000; Full time

Job summary

A leading company in clinical research is seeking a Clinical Project Manager/Senior Clinical Project Manager to oversee global clinical trials in Oncology. The role involves managing project delivery, client relationships, and cross-functional teams in a dynamic environment. Ideal candidates will have significant experience in clinical trial management and Oncology studies, with strong organizational and communication skills.

Qualifications

• 5-7 years industry experience, with at least 3 years in full-service clinical trial management.
• Experience managing Oncology studies.

Responsibilities

• Lead clinical projects independently, managing budgets and scope.
• Act as the primary client liaison, providing excellent service.
• Manage all aspects of clinical trials across functional areas.

Skills

Communication

Organizational Skills

Interpersonal Skills

Education

Degree in life sciences

Tools

MS Office

MS Project

PowerPoint

CTMS

eTMF

EDC

IXRS

Job description

Clinical Project Manager / Senior Clinical Project Manager

Remote, United Kingdom

Are you an experienced full-service Project Manager in clinical trials, passionate about advancing research and development in Oncology? Do you take a consultative approach to trial management and value being a key partner in operational delivery?

Precision for Medicine (CRO) seeks to hire a (Senior) Project Manager with Oncology experience, having managed full-service clinical trials within a CRO environment, to join our global team.

This role provides full oversight of clinical projects across global/regional (Ph I-IV) trials in Oncology (or Rare Diseases or CNS). You will be accountable for project delivery, overseeing all functional departments, and ensuring timelines, scope, cost, and quality standards are met.

You will be involved in all study stages, including proposal strategy, development, costing, bid defense, and managing studies through to completion, including client relationships, project team, budget, and timelines.

You will work within a cross-functional team with internal and external stakeholders, driving quality and coordinating study activities.

We offer a dynamic, collaborative environment with dedicated team members who thrive on challenges, attention to detail, and adaptability. If you are proactive and team-oriented, this opportunity is for you.

How we support your growth:

• Lead clinical projects independently, managing budgets and scope, using your interpersonal and organizational skills to meet objectives, including international trials.
• Act as the primary client liaison, providing excellent service and participating in proposal activities and presentations.
• Coordinate with project teams and senior management, including C-level stakeholders.
• Manage all aspects of clinical trials across functional areas such as data management, safety, clinical, medical monitoring, and biostatistics.
• Prepare project status updates, identifying key deliverables, performance metrics, and escalation procedures.
• Contribute to efficient trial management as an active project team member.
• Develop and review protocols, study documentation, project plans, informed consents, site contracts, and budgets.

Requirements:

• Degree or equivalent in life sciences or related field.
• Experience in a full-service/global Project Management role within a CRO.
• 5-7 years industry experience, with at least 3 years in full-service clinical trial management.
• Experience managing Oncology studies.
• Knowledge of GCP/ICH guidelines and clinical development processes.
• Willingness to travel domestically and internationally, including overnight stays.
• Fluent in English, both written and spoken.
• Proficiency in MS Office, MS Project, PowerPoint, and experience with CTMS, eTMF, EDC, IXRS.
• Ability to foster positive working relationships internally and externally.
• Understanding of medical terminology and clinical trial activities related to development plans.

At Precision for Medicine, we combine innovative clinical trial designs, leading operational and medical expertise, advanced biomarker and data analytics, and a passion for rare diseases and oncology.

We are a people-focused CRO with a supportive, collaborative environment that promotes work-life balance and team development.

Join us to contribute to groundbreaking cancer therapies and be part of a growing organization that values your contributions daily.

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We are 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 protected characteristics.

If you require accommodations during the application process due to a disability, please contact [e-mail].

Beware of fraudulent job offers; our company will only extend offers after proper communication and interviews with our recruiting team.