Description
A mid sized pharmaceutical company is seeking an experienced CPM/ CTM to help manage an oncology studyThis is a great opportunity for those interested in utilizing and expanding their oncology clinical trials management experience. The candidate will be accountable for initiating and overseeing all activities from study start-up to close out.
This person will be responsible for:
- CRF design and review, study manual design and review
- Oversight of vendor start up
- Managing and facilitating site start-up activities, monitoring sites as needed
- Clinical supplies
- Personnel management
- Managing site enrollment and patient tracking
- Review of CRF queries, protocol deviations, and ensuring quality data
- Serving as the point of contact to sites and vendors
This ideal candidate will have the following qualifications:
- BA/ BS in a life science or related field.
- 3+ years of clinical project management experience.
- Experience managing and overseeing all processes of involved in a global clinical trial.
- Experience managing Phase II and Phase III clinical trials.
- Experience in Oncology research.
- Previous monitoring experience.
This job is located in South San Francisco, CA. There is no option to work remotely.
This is an immediate hire position. We are currently conducting phone interviews.
To find out more about Real please visit www.realstaffing.com