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Summary
About the Role
About You
- Bachelor's degree in a life science; advanced degree is a plus.
- Minimum 12 years of clinical experience in biopharma, CRO, or healthcare, with at least 5 years managing cross-functional project teams.
- Proven expertise in overseeing clinical trials and managing clinical programs.
- Monitoring experience.
- Experience with BLA submissions and regulatory agency inspections.
Benefits
- Opportunity to work in a diverse and inclusive environment.
- Engagement in meaningful work that impacts patients' lives.
bluebird bio is pursuing curative gene therapies to give patients and their families more bluebird days. With a dedicated focus on severe genetic diseases, bluebird has industry-leading programs for sickle cell disease, β-thalassemia and cerebral adrenoleukodystrophy and is advancing research to apply new technologies to these and other diseases. We custom design each of our therapies to address the underlying cause of disease and have developed in-depth and effective analytical methods to understand the safety of our lentiviral vector technologies and drive the field of gene therapy forward. Founded in 2010, bluebird has the largest and deepest ex-vivo gene therapy data set in the world—setting the standard for the industry. Today, bluebird continues to forge new paths, combining our real-world experience with a deep commitment to patient communities and a people-centric culture that attracts and grows a diverse flock of dedicated birds. Community guidelines: http://bit.ly/bbbGuidelines