Upvote
Downvote
Vice President, Clinical Development
Share Job
- Suggest Revision
- The position represents a key partner in establishing and driving forward tactical plans to enable Editas to deliver on its mission to translate the power and potential of genome editing into a broad class of in-vivo and cellular treatments that transform lives of people living with serious diseases.
- As a key strategic functional leader, the incumbent will work across a matrixed organization with Research, Clinical Operations, Regulatory, Biometrics and other functions to ensure integrated development strategies.
- He/She will be a key Editas spokesperson at external meetings, including regulatory interactions and scientific meetings and partner with Medical Affairs, Commercial and Corporate Communications in setting external messaging and communication strategies.
- He/She will lead a group of physicians and clinical scientists who have responsibility for conceiving, delivering, and overseeing Phase 1-3 trials progressing from pre-IND activities to BLAs, establishing plans for long-term follow up and pharmacovigilance, and is responsible for protocol development and clinical sections of regulatory documents (e,g.
- Collaborate closely with Non-clinical, Regulatory, Clinical Operations, CMC and Biometrics to ensure tight strategic integration of product development plans and strategies.
Active Job
Updated 11 days agoSimilar Job
Relevance
Active