Provide leadership and oversight for clinical trial activities, ensuring operational efficiency, meeting global regulatory standards, as well as contributing to the overall success of Protara’s clinical programs. Collaborate with internal stakeholders, CROs, vendors, and external parties to ensure the timely and cost-effective completion of clinical trials.

As Principal Clinical Scientist, you will drive the scientific planning, strategy, and clinical management of DELFI Sponsored studies and external research collaborations from early development through publication. You will lead completion of study deliverables through active participation in all aspects of study design, execution, analysis and reporting. You will also manage study deliverables and milestones.