Clinical Project Manager / Senior Clinical Project Manager

Precision Medicine Group; Greater London; Presencial; GBP 70 000 - 100 000; Tempo integral

Resumo da oferta

Precision for Medicine is seeking an experienced Clinical Project Manager/Senior Clinical Project Manager with Oncology expertise to lead full-service trials in a CRO setting. You will oversee global/regional studies (Phase I-IV), manage client relationships, project teams, budgets and timelines across the full study lifecycle.

You will liaise with stakeholders, drive quality, and ensure delivery of study plans, cost control, and timelines.

Qualificações

• Degree or life-science qualification required.
• Previous experience in a full-service/global Project Management role in CRO.
• Experience in Oncology studies.
• Familiar with GCP/ICH and clinical development processes.
• Willingness to travel domestically and internationally.
• Strong English written and spoken communication.
• Excellent presentation skills.
• Proficient with MS Office suite and trial systems (CTMS, eTMF, EDC, IXRS).
• Ability to build positive working relationships and understand medical terminology.

Responsabilidades

• Lead independently clinical projects within budget and scope, including international trials.
• Be primary client liaison, supporting proposals and presentations.
• Coordinate with project team and senior management across Precision and sponsors.
• Oversee all aspects of trials across data management, safety, medical monitoring, and biostatistics.
• Prepare status updates and define key deliverables and metrics of success.
• Contribute to efficient trial management as a core project team member.
• Prepare and review protocols, study documentation, site contracts, and budgets.

Conhecimentos

Global PM leadership

Oncology experience

GCP/ICH knowledge

Travel readiness

English communication

Client liaison/presentation

MS Office/MS Project/PowerPoint

CTMS/eTMF/EDC/IXRS proficiency

Medical terminology

Cross-functional coordination

Formação académica

Life science degree

Ferramentas

MS Office

MS Project

PowerPoint

CTMS

eTMF

EDC

IXRS

Descrição da oferta de emprego

Are you an experienced full service Project Manager in the field of clinical trials who’s engaged in addressing the challenges facing the research and development of novel compounds in Oncology? Are you passionate about impacting the health and lives of patients around the world? Do you take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery?

Precision for Medicine is looking to hire a Clinical Project Manager / Senior Clinical Project Manager with experience in Oncology who has managed full service clinical trials within a CRO setting to join our global team.

In this pivotal role you will have full service oversight for clinical projects across global/regional (Phase I-IV) trials within Oncology. You will be accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality.

Involved in all study stages, including proposal strategy, development, costing, and bid defence, you will see studies through the full cycle to completion, managing the client relationship, project team and budget and timelines throughout.

You will work in a cross‑functional team with both internal and external stakeholders, driving quality and coordinating the study team.

We offer an amazing high‑energy, dedicated, collaborative team environment where team members thrive on challenge, detail and dynamic conditions. If you are no stranger to taking charge and seek positive teamwork to deliver extraordinary work, we have an opportunity for you.

We will keep you busy and support your growth

• Independently lead clinical projects in accordance with the study budget and scope of work; use strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects, including financial objectives. You may be called upon to run international trials as well.
• Serve as the primary point‑of‑contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations.
• Liaise with Project Team and senior management of both Precision and sponsors, including C‑level stakeholders.
• Handle and lead all aspects of a clinical research trial or trials.
• Own total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
• Prepare project status updates for clients and management; identify key deliverables and performance metrics of success and escalation.
• Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials.
• Prepare and review protocols and other study documentation such as project plans, information consents, site contracts and budgets.

Requirements

• Degree or similar related life science qualification, or equivalent combination of education and experience.
• Previous experience in a full‑service/global Project Management role working in the CRO industry is essential.
• Extensive experience working within Clinical Operations position within a CRO, and at least 4 years full‑service Project Management experience in a clinical trial setting working for a Clinical Research Organisation.
• Experience managing studies within Oncology.
• Working understanding of GCP/ICH guidelines and the clinical development process.
• Ability to drive and availability for domestic and international travel including overnight stays.
• Be able to communicate effectively in the English language, both written and spoken.
• Strong presentation skills.
• Proven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS).
• Proven ability to develop positive working relationships with individuals and teams internally and externally.
• Demonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan.

Precision for Medicine's uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry‑leading operational and medical authorities, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.

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

We invite you to learn more about our growing organization serving our clients that are researching ground‑breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day.

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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].

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