Director of Research Operations

Responsibilities

• Collaborates with executive leadership and principal investigators to provide strategic oversight of the clinical research program.
• Develops, directs, implements, and evaluates research strategies in coordination with internal departments supporting clinical trial operations.
• Oversees multi-site research operations and staff to ensure compliance with applicable SOPs and ICH-GCP guidelines.
• Leads preparation and implementation of research budgets and financial reporting across all research sites.
• Partners with senior leadership to establish accrual targets and financial performance objectives.
• Establishes accountability standards across all locations to support achievement of enrollment and financial goals.
• Prepares and presents financial and operational research reports for executive leadership and governance committees.
• Provides high-level strategic leadership to improve clinical trial processes, efficiency, and overall program effectiveness.
• Serves as a liaison between corporate research operations, committees, and clinical sites to communicate initiatives, updates, and operational issues.
• Provides oversight of research governance, including SOPs, policies, and procedural compliance.
• Supervises, trains, and mentors research staff while supporting ongoing professional development and continuing education initiatives.
• Promotes a strong research culture by collaborating with physicians and leadership to support program growth and engagement.
• Works with research leadership and physicians to evaluate and select appropriate studies for program participation.
• Supports promotion and awareness of the research program within the organization, community, and referring providers.

Qualifications

• Bachelor’s degree in a clinical, scientific, or related field preferred; BSN preferred for nursing professionals.
• Minimum of 7 years of clinical research experience, preferably in oncology.
• Minimum of 7 years of progressive leadership and supervisory experience in a clinical environment; clinical research leadership strongly preferred.
• Current RN licensure required where applicable.
• Strong leadership skills with the ability to function effectively in a matrixed environment.
• Excellent communication, organizational, and interpersonal skills with the ability to manage multiple priorities in a fast-paced setting.
• Proficiency in standard computer applications (e.g., Microsoft Office Suite, Excel).
• Strong knowledge of GCP and ICH guidelines.
• Ability to interpret clinical and regulatory documents including protocols, informed consent forms, and study materials.
• Working knowledge of medical terminology and clinical disciplines relevant to oncology research (e.g., diagnostics, pathology, pharmacology, hematology).
• Basic understanding of financial management including budgeting, contracting, and site-level revenue cycle concepts.