Associate Director, Regulatory CMC – Global Submissions Leader

A leading biopharmaceutical company in Carmel, Indiana, is seeking a Regulatory Affairs professional to support global regulatory CMC activities. This role involves collaborating on submissions for clinical programs and managing CMC regulatory strategies. The ideal candidate will have over 10 years of pharma or biotech experience and at least 7 years directly in regulatory CMC. This is a chance to contribute to significant development efforts in a dynamic biotech setting. #J-18808-Ljbffr