Principal investigator or sub-investigator for Phase I and clinical pharmacology studies.
- With support of management, present approved protocols, informed consents, and associated documents to members of the IRB
- Transmit all pertinent study-related information to the IRB
- May manage exempt and/or non-exempt direct reports, and project related functional reports
- May lead other staff members in managing 3xempt and/or non-exempt direct reports, and project related functional reports
- Act as a resource to support other AbbVie functional areas and employees as appropriate
- Medical Doctor with active Illinois medical license in good standing
- Independent clinical practice experience
- Medical specialty board eligibility or certification