Overview In this role you lead full-service clinical projects in oncology within a CRO setting, overseeing global/regional trials from proposal through completion. You will coordinate cross-functional teams, manage client relationships, budgets, and timelines, and ensure quality and adherence to scope. The position offers a high-energy, collaborative environment with growth opportunities and exposure across study stages. You drive delivery and performance, collaborating with internal and sponsor teams to advance precision oncology trials.
Pay / Benefits - work-life balance
- collaborative environment
- team development
- growth opportunities
Responsibilities - Lead full-service clinical projects within global/regional (Ph I–IV) oncology trials
- Act as primary client liaison and contribute to proposals, strategy, costing, and bid defence
- Oversee all functional areas (data management, safety, clinical, medical monitoring, biostatistics)
- Prepare and present project status updates and performance metrics
- Coordinate study team efforts and ensure timely delivery within budget and scope
- Develop and review protocols and study documents (plans, informed consents, budgets, contracts)
Key requirements - CRO background with full-service/global PM experience in clinical trials
- Experience in oncology trials
- GCP/ICH knowledge and clinical development process understanding
- Ability to travel domestically and internationally
- Strong English communication and presentation skills
- Proven computer skills (MS Office, MS Project, PowerPoint) and systems (CTMS, eTMF, EDC, IXRS)
- Ability to build positive working relationships with internal and external teams
- Understanding of medical terminology and trial activities in a development plan
- strong interpersonal and organizational skills
- client-focused and service-oriented
- cross-functional collaboration
- CTMS
- eTMF
- EDC
