Associate Director, Clinical Science

Role Summary

Associate Director, Clinical Science. Oversees all clinical aspects of clinical trials, including planning and authoring clinical deliverables, routine medical monitoring, site interactions, and presenting data. Works cross-functionally to ensure study protocols are executed and data quality is high. Handles multiple early-phase projects in a fast-paced environment.

Responsibilities

• Create – Serve as the authoring lead on multiple clinical documents, including IND and study-specific documents, and manage site/agency interactions.
• Collaborate - Lead and contribute within dynamic teams, guiding decisions and timelines as needed.
• Drive & Deliver – Ensure study data quality, review medical monitoring, issue and close queries, review TLFs, summarize data, and present data to management; present protocol procedures and Site Initiation Visits.
• Prioritize – Support multiple early-phase (1-2) studies simultaneously with strong time management and organizational skills.

Qualifications

• 5+ years as a Clinical Scientist in a pharmaceutical or biotech company
• Prior experience in early phase 1-2 oncology studies is required
• Experience with hematologic malignancies is preferred
• Strong interpersonal and communication skills (spoken and written)
• Strong relationship-building skills across disciplines and levels
• Proven ability to manage multiple, complex, competing priorities
• Ability to operate strategically and tactically
• Problem solving and issues management with a solution-focused approach

Skills

• Clinical trial design and document authoring
• Medical monitoring and data review
• Cross-functional collaboration and stakeholder management
• Data presentation and communication
• Project and time management

Education

• Not specified in provided description

Additional Requirements

• Working Location: Hybrid role in Salt Lake City / New York City office; in-office at least 50% of the time