Clinical Trial Manager, Oncology Job Description Template
Our company is looking for a Clinical Trial Manager, Oncology to join our team.
Responsibilities:
- Assist PM with preparation of information for inclusion in monthly report to client;
- Define the scope of work with the client and clinical monitoring team;
- Assist PM in identifying and generating changes in scope and notify client of potential changes in scope;
- Assist PM in review of project budgets, monitoring costs, potential overruns and propose/implement cost effective solutions;
- Assist PM in preparation of audit responses, as appropriate;
- Serve as client advocate within IQVIA Biotech;
- Review and approve CRA travel expenses and time sheets;
- Ensure all project documentation is appropriately filed per IQVIA Biotech SOPs;
- Develop and implement Clinical Monitoring Plan;
- Assure that the appropriate IQVIA Biotech and/or sponsor SOPs are followed.
Requirements:
- Ability to manage 2 studies at once;
- 2+ recent years of experience working on Oncology trials;
- Knowledge of ICH-GCP;
- Experience with global studies;
- 3-5+ recent years working as a Clinical Trial Manager;
- Bachelor’s degree or higher in related scientific subject;
- Phase 1 Dose Escalation experience.