Job Description
Responsible for assigned clinical trials being managed to the highest standards. Accountable for the performance and delivery of all trial activities, including oversight and management of complex, cross-functional study level issues. Point of escalation for study teams you will work with cross-functional partners and vendors to discuss issues, develop solutions, follow through resolution, and implement process improvements. You will proactively communicate complex and sensitive study information or issues and understands stakeholder impact. Candidate must have a bachelor’s degree, in a life science with a minimum 7 years clinical experience (biopharma, CRO, healthcare), with at least 2 years of managing cross-functional project teams. Monitoring experience preferred.
About Bluebird Bio
At bluebird every role has meaning, every team member is respected, and every day is a chance to fly higher.