Clinical Project Manager

Summary

Join Precision for Medicine (CRO) as a (Senior) Project Manager and play a pivotal role in the research and development of novel oncology compounds. You will provide full-service oversight for clinical projects across global/regional (Phase I-IV) trials, ensuring adherence to timelines, scope, cost, and quality. Responsibilities include proposal strategy, development, costing, bid defense, client relationship management, and project team leadership. You will collaborate with cross-functional teams, both internal and external, driving quality and coordinating study execution. This position requires a life science degree or equivalent, extensive experience in full-service project management within a CRO setting, and a strong understanding of GCP/ICH guidelines. The ideal candidate will have experience managing oncology studies and possess excellent communication and presentation skills.

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

Benefits

Supportive and collaborative environment which promotes work life balance and encourages team development