Responsibilities
- 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 in the execution of the projects; both contracted objectives and financial objectives.
- 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.
- Provide 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 review protocols and other study documentation such as project plans, inform consents, site contracts and budgets.
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.
- 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 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.
Work Arrangement
Remote (Worldwide)
Additional Information
- Availability for domestic and international travel including overnight stays.
- Communicate effectively in the English language both written and spoken.
