Senior Project Manager - Clinical Trials
Remote, United Kingdom
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 (Senior) Project Manager ideally 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 (or Rare Diseases or CNS). You will be accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality.
You will be involved in all study stages, including proposal strategy, development, costing, and bid defence, and 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.
Primary Responsibilities
- Lead clinical projects independently in accordance with the study budget and scope of work, using strong interpersonal and organisational skills to set and achieve both contracted and financial objectives. You may also be called upon to run international trials.
- 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 the Project Team and senior management of both Precision and sponsors, including C‑level executives.
- Handle and lead all aspects of a clinical research trial or trials.
- Provide total project management for all functional areas, including data management, safety, clinical, medical monitoring and biostatistics.
- Prepare project status updates for clients and management, identifying key deliverables and performance metrics of success and escalation.
- Serve as an active member of the Project Team with the goal of contributing toward efficient management and execution of trials.
- Prepare and review protocols and other study documentation such as project plans, informed consents, site contracts and budgets.
Requirements
- Degree or a similar related life‑science qualification, or an equivalent combination of education and experience.
- Previous experience in a full‑service/global Project Management role working in the CRO industry is essential.
- 5 to 7 years of industry experience and at least 4 years of 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.
- Ability to communicate effectively in the English language, both written and spoken.
- 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 both 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 Group is a people‑focused CRO with a supportive and collaborative environment that promotes work‑life balance and encourages team development.
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, colour, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
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