Role Summary
As an Associate Director, Clinical Science, you will oversee all clinical aspects of one or more early‑phase trials. You will author and review clinical deliverables (protocols, amendments, medical monitoring plans, annual reports, study-specific updates, CSRs), perform routine medical monitoring, manage site communications, and present findings to internal and external stakeholders. You will collaborate cross-functionally to ensure study protocols are executed accurately and that data are clean and actionable. Location: Salt Lake City / New York City, hybrid with in‑office 50% of the time.
Responsibilities
- Authoring lead on multiple clinical documents, including INDs and study-specific documents, with site and agency interactions.
- Collaborate with dynamic cross-functional teams, leading or contributing to decisions and timelines to advance projects.
- Drive & Deliver: ensure study data quality by medical monitoring, reviewing and closing queries, reviewing TLFs, summarizing data, and presenting data to management; present protocol procedures and Site Initiation Visits (in-person or virtual).
- Prioritize: support multiple early-phase (1–2) studies concurrently, requiring strong time management and organizational skills.
Qualifications
- Required: 5+ years as a Clinical Scientist in a pharmaceutical or biotech company.
- Required: Prior experience in early phase 1-2 oncology studies.
- Preferred: Experience with hematologic malignancies.
- Required: Strong interpersonal and communication skills (spoken and written) with ability to effectively communicate on project planning, progress, tracking, etc.
- Required: Strong relationship-building skills to work effectively with others in various disciplines and levels.
- Required: Proven ability to manage multiple, complex, and competing priorities to effective and efficient conclusions.
- Required: Ability to operate strategically and tactically.
- Required: Proven ability in problem solving and issues management that is solution-focused.