Senior Clinical Project Manager - Oncology
New
P
Precision for MedicineClinical trials
Remote, United KingdomFull-TimeSenior
Salary not disclosed
Apply NowOpens the employer's application page
Job Details
- Languages
- Be able to communicate effectively in the English language both written and spoken
- Experience
- At least 4 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation
- Required Skills
- MS OfficePowerPoint
Requirements
- Hold a degree or similar related life science qualification, or have an equivalent combination of education and experience.
- Have previous full-service/global project management experience in the CRO industry.
- Have extensive experience in a clinical operations position within a CRO.
- Have at least 4 years of full-service project management experience in a clinical trial setting at a Clinical Research Organisation.
- Have experience managing oncology studies.
- Have a working understanding of GCP/ICH guidelines and the clinical development process.
- Be able to communicate effectively in spoken and written English.
- Have strong presentation skills.
- Have computer skills with MS Office, MS Project, and PowerPoint.
- Have experience with CTMS, eTMF, EDC, and IXRS software.
- Be able to drive and travel domestically and internationally, including overnight stays.
Responsibilities
- Lead clinical projects in line with study budgets, scope of work, contracted objectives, and financial objectives.
- Serve as the primary client contact, including participating in proposal activities and client presentations.
- Liaise with project teams and senior management at Precision and sponsor organizations.
- Manage all aspects of clinical research trials.
- Oversee project activities across functional areas, including data management, safety, clinical, medical monitoring, and biostatistics.
- Prepare project status updates for clients and management, identifying key deliverables, performance metrics, and escalations.
- Contribute to efficient management and execution of clinical trials as an active project team member.
- Prepare and review protocols and study documents, including project plans, informed consents, site contracts, and budgets.
View Full Description & ApplyYou'll be redirected to the employer's site
