• Plan and facilitate meeting and committees to address clinical research issues.
• Proactively handle standards of care issues or conflict of interest issues.
• Serve as Principal Investigator on Clinical Trials as requested, in accordance with the
requirements set forth FDA Form 1572, SCRI's policies and procedures and
applicable law.
• Act at all times in accordance with the SCRI/McKesson Code of Conduct and
Mission and Values statement.
• Perform other duties as
assigned. Qualifications:
• Moderate to high level of experience in the field.
• Regionally or nationally known in the field.
• Has publications in peer reviewed journals and speaking experience.
• Has served in the primary leadership role on multiple clinical trials.
• Some experience in providing strategic executive level input to companies.
