Key Responsibilities:
- Oversee CRO programming activities, including SDTM, ADaM and other deliverables.
- Review CRO programming plans, specifications, datasets, outputs, and QC documentation.
- Collaborate with Data Management to support data cleaning, external data review, and database lock.
Required Experience & Skills:
- At least 10 years of experience in clinical statistical programming.
- Strong expertise in SAS, CDISC SDTM/ADaM standards and regulatory submission requirements.
- Strong written and verbal communication skills with a collaborative approach.
Preferred Experience & Skills:
- Prior experience as programming lead or submission programming lead.
- Experience overseeing multiple studies or programs in parallel.
- Ability to read/communicate in Chinese is helpful.
Braveheart Bio
Braveheart Bio is a Bay Area–based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease. They have a proven leadership team, a strong financial foundation, and a high-value late-stage asset, making it an outstanding opportunity for mission-driven professionals.