Medical Director — Clinical Trials Leader

AL Solutions; Tampa (FL); On-site; USD 180,000 - 240,000; Full time

Job summary

AL Solutions is seeking a Medical Director to lead medical oversight at a Tampa research site. You will supervise medical activities, support protocol execution, and develop a high‑performing team while ensuring participant safety and data integrity.

You will collaborate with investigators, sponsors, and CRO partners, guiding protocol feasibility and contributing medical input to study development in a fast-paced regulatory environment.

Qualifications

• Licensed MD or relevant doctoral qualification with transferable experience.
• Minimum of two years' clinical trial management and oversight experience.
• Strong knowledge of FDA regulations and Good Clinical Practice (GCP).
• Ability to lead people, communicate clearly, and build effective working relationships.
• Proven ability to manage multiple studies and competing priorities in a fast-paced research environment.
• Independent, proactive approach with commitment to participant safety and research quality.

Responsibilities

• Oversee site medical activities, support protocol execution, and ensure data integrity.
• Lead recruitment, training, and supervision of investigators and clinical personnel.
• Assess protocol feasibility and provide medical input to protocol development as needed.
• Drive site process improvements and strengthen quality programs.
• Participate in study initiation meetings, monitoring visits, and audits.
• Ensure adherence to FDA regulations, ICH-GCP, and site procedures.
• Partner with leadership on staffing, resources, timelines, and site performance.

Skills

Leadership

Regulatory knowledge

Communication

GCP knowledge

Clinical trial mgmt

Education

MD or doctoral qualification

Job description

AL Solutions is seeking a Medical Director to lead medical oversight at a Tampa research site. You will supervise medical activities, support protocol execution, and develop a high‑performing team while ensuring participant safety and data integrity.

You will collaborate with investigators, sponsors, and CRO partners, guiding protocol feasibility and contributing medical input to study development in a fast-paced regulatory environment.