Description
Overview:This role requires an experienced Clinical Operations Manager that can assist a study team with global start up activities such as ICF and contract review and vendor management. This person may also be involved in Investigator Meeting planning activities and SOP gap analysis. This person should be able to complete study start up activities with minimal supervision/direction. This person may also act as a mentor to junior staff.Requirements:
- Clinical trial experience with ONCOLOGY (5+ yrs)
- Experience with Phase III clinical trials (5+ yrs)
- International clinical trial experience (3+ yrs)
- Past success in a study manager position
Additional Information:
- Type: contract
- Length: 18 months, renewable
- Rate: depends on experience. range: 60-100
- ***This is an in-house role with minimal travel
To find out more about Real please visit www.realstaffing.com