Associate Director, Clinical Science

Role Summary

Associate Director, Clinical Science – oversee all clinical aspects of clinical trials, authoring clinical deliverables, medical monitoring, site interactions, and cross-functional collaboration to ensure high-quality study data in early-phase oncology programs.

Responsibilities

• Create ‚Äì Serve as the authoring lead on multiple clinical documents, including IND and study-specific documents, and manage site/agency interactions.
• Collaborate ‚Äì Work with dynamic cross-functional teams, leading decisions or contributing expertise to advance tasks.
• Drive & Deliver ‚Äì Ensure the quality of study data, review medical monitoring, issue and close queries, review tables, listings, and figures, summarize data, and present data to management; present protocol procedures and Site Initiation Visits in-person and virtually.
• Prioritize ‚Äì 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) for project planning and progress tracking.
• Strong relationship-building skills across disciplines and levels.
• Proven ability to manage multiple, complex, and competing priorities to a successful conclusion.
• Ability to operate both strategically and tactically.
• Proven problem-solving and issues-management skills with a solution-focused approach.

Skills

• Clinical trial operations
• Medical monitoring and data review
• IND and regulatory document authoring
• Cross-functional collaboration
• Data presentation and communication

Education

• Not specified in the source.

Additional Requirements

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