Senior Project Manager - Clinical Trials

Precision Medicine Group; United Kingdom; On-site; GBP 50,000 - 80,000; Full time

Job summary

Precision Medicine Group is seeking an experienced (Senior) Project Manager to oversee clinical trials, primarily in Oncology. The ideal candidate will have 5-7 years of experience in Project Management, particularly within a CRO setting, and must excel in communication and organizational skills. Responsibilities include managing project delivery from start to finish, serving as the primary client liaison, and collaborating with interdisciplinary teams. Strong understanding of GCP/ICH guidelines is essential for this role. The position offers opportunities for domestic and international travel.

Qualifications

• 5 to 7 years industry experience with at least 4 years in Project Management for clinical trials.
• Experience managing studies within Oncology.
• Working understanding of GCP/ICH guidelines.

Responsibilities

• Independently lead clinical projects according to budget and scope.
• Serve as the primary contact with clients for project updates.
• Prepare and review project status updates and documentation.
• Manage all functional areas of clinical trials.

Skills

Project Management

Communication

Interpersonal Skills

Presentation Skills

Education

Degree in life sciences or equivalent

Tools

MS Office

MS Project

CTMS

eTMF

EDC

IXRS

Job description

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 are looking to hire a (Senior) Project Manager ideally with experience in Oncology who have 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 (ph I-IV) trials, within Oncology (or Rare Diseases or CNS). 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, and seeing 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 that thrives on detail and embraces dynamic challenges. If you are no stranger to taking charge and seeking positive teamwork to deliver extraordinary work, we have an opportunity for you.

How we will keep you busy and support your growth

• You will independently lead clinical projects in accordance with the study budget and scope of work. You will use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and 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.
• Handle and lead all aspects of a clinical research trial or trials.
• 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; identifying 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, informed 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.
• 5 to 7 years industry experience 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 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.