About this role
About the Role The Clinical Project Manager / Senior Clinical Project Manager will provide full-service oversight for oncology trials (Ph I-IV) in a CRO setting, leading global and regional projects. You will be accountable for clinical project delivery, oversight of all functional departments, and ensuring timelines, scope, cost and quality. You will work with internal and external stakeholders across the trial lifecycle from proposal strategy to final study completion. What You'll Do
- 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; may 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; 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, informed consents, site contracts and budgets. What We're Looking For
- 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.
- 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.
- Able to communicate effectively in English (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.