As a Senior Clinical Scientist, you will provide scientific and clinical support from ongoing early and late-stage clinical trials with an emphasis on protocol-specific, in-life clinical data monitoring activities. This role will also serve as a point of contact for CROs, investigators and study staff in day-to-day safety monitoring. The position requires experience in analysis and interpretation of clinical data.

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.

The Clinical Data Manager is a key member of the Clinical team and will be responsible for assisting with the deliverable oversight and management of our Biometrics partners related activities conducted for clinical trials conducted by Vaxcyte, from study start-up through to study closeout, ensuring high quality data deliverables which are on time and within budget.