About The Position

M3 Wake Research is hiring a Regional Director to lead clinical operations across a region of its site network. This remote leadership role oversees Site Directors and Site Managers, partners closely with principal investigators, and ensures sites meet enrollment, quality, and revenue goals. The position requires up to 50% travel and involves building accountable teams and keeping clinical trials running smoothly.

Requirements

  • Bachelor’s degree in science, nursing, or a related field; an equivalent combination of education, experience, and training is considered.
  • 7–10+ years of progressively responsible experience in clinical research or related operations.
  • Clinical experience across two or more therapeutic areas.
  • Strong knowledge of FDA regulations, ICH-GCP, safety reporting, and investigational product handling.
  • Healthcare background in a line of business involving direct patient care and physician collaboration.
  • Comfort making financially sound, defensible business decisions.
  • Strong communication skills across sites, sponsors, CROs, and regulators.
  • Data-driven approach and a track record of developing and coaching talent.

Nice To Haves

  • Five or more years of people management experience preferred.
  • Experience with multi-site networks, SMOs, TMOs, or hospital-owned physician networks preferred.
  • Prior experience managing teams or site operations.

Responsibilities

  • Lead, coach, and develop Site Directors and Site Managers by setting clear goals, KPIs, and expectations.
  • Step in as Interim Site Director or arrange coverage when a site is in transition.
  • Monitor site operations and performance metrics to improve efficiency, quality, enrollment, and protocol compliance.
  • Implement network-wide processes, systems, and SOPs consistently across sites.
  • Partner with site leadership on budgeting, forecasting, FTE planning, and margin management.
  • Review financial and operational reports to identify risks and trends.
  • Work with Marketing and Participant Recruitment to strengthen enrollment strategy and forecasting.
  • Support Business Development with feasibility input and site capability assessments.
  • Work with Quality, Regulatory, and Clinical Affairs on audit readiness and principal investigator oversight.
  • Build relationships with principal investigators and serve as the regional escalation point for investigator and sponsor concerns.
  • Support hiring, onboarding, and staffing decisions for site-level teams.
  • Lead mid-year and annual performance reviews for direct reports.

Benefits

  • Competitive wages
  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Disability insurance
  • Employee assistance program
  • Flexible spending account
  • Health insurance
  • Life insurance
  • Paid time off
  • Vision insurance
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