About this role
About the Role Precision for Medicine is hiring a Clinical Project Manager / Senior Clinical Project Manager with Oncology focus to oversee full-service global/regional (Ph I-IV) trials within Oncology in a CRO setting. You will be accountable for clinical project delivery, oversight of all functional departments, and ensuring timelines, scope, cost and quality.
Involved in all study stages, including proposal strategy, development, costing, and bid defence, and guiding studies through the full cycle to completion, managing the client relationship, project team and budget and timelines throughout.
We offer a high-energy, collaborative environment and opportunities for professional growth. What You'll Do
- Independently lead clinical projects in accordance with the study budget and scope of work; international trials may be required.
- Serve as the primary client liaison, providing excellent customer service, and participate in proposal activities and client presentations.
- Liaise with 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; total project management for data management, safety, clinical, medical monitoring and biostatistics, etc.
- Prepare project status updates for clients and management; identify key deliverables and performance metrics and escalation.
- Be an active member of the Project Team, contributing to efficient management and execution of trials.
- Prepare and review protocols and study documents such as project plans, informed consents, site contracts and budgets. What We're Looking For
- Degree or 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.
- Extensive experience working within Clinical Operations position within a CRO, and at least 4 years full-service Project Management experience in a clinical trial setting.
- Experience managing Oncology studies.
- Working understanding of GCP/ICH guidelines and the clinical development process.
- Ability to drive and availability for domestic and international travel including overnight stays.
- English language proficiency (written and spoken) with strong presentation skills.
- Proficient 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.
- Experience with oncology and precision medicine would be a plus.