Clinical Project Manager

Summary

Join Precision for Medicine (CRO) as a (Senior) Project Manager, ideally with Oncology experience, to oversee full-service clinical projects (Phases I-IV) globally/regionally. You will be accountable for clinical project delivery, managing all functional departments, and ensuring adherence to timelines, scope, cost, and quality. Responsibilities include proposal strategy, development, costing, bid defense, client relationship management, and project team/budget oversight. You will work in a cross-functional team, driving quality and coordinating the study team. This role requires strong interpersonal and organizational skills, experience managing international trials, and excellent customer service. Precision for Medicine offers a collaborative and supportive environment.

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 3 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 individual 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

Responsibilities

• Independently lead clinical projects in accordance with the study budget and scope of work
• Use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and financial objectives
• 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 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 reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets