What are the responsibilities and job description for the AD Clinical Pharmacology position at GQR?
Position : Associate Director, Clinical Pharmacology
Location : South San Francisco (Hybrid, 3 days onsite)
About the Role
Our client, a late-stage biopharmaceutical company, is seeking an Associate Director of Clinical Pharmacology to play a critical role in advancing innovative therapies for fibrotic diseases and oncology. This individual will lead the design, execution, and strategic oversight of clinical pharmacology plans, supporting both a late-stage fibrosis program and an early-stage oncology program.
This is a hybrid position based in South San Francisco , requiring three days onsite each week.
Key Responsibilities
- Act as Study Director for Phase 1 studies, ensuring high-quality and timely execution.
- Develop clinical pharmacology plans and contribute to regulatory submissions (e.g., INDs, NDAs).
- Collaborate with cross-functional teams and oversee modeling and simulation activities at CROs.
- Author and review clinical and regulatory documents, including protocols, statistical analysis plans, and study reports.
- Serve as the subject matter expert for clinical pharmacology during regulatory meetings.
- Ensure compliance with GCP and global regulatory guidelines.
Qualifications
Compensation
The annual base salary for this role is $205,000–$215,000 , plus performance-based bonuses. Additional equity and benefits will be provided.
Note : Our client is not offering visa sponsorship or transfer at this time.
If you're looking for a role where you can shape clinical pharmacology strategies and contribute to cutting-edge therapeutic programs, apply today!
Salary : $205,000 - $215,000
