Clinical Research Site Director - Lead Patient Trials

ObjectiveGI, Inc.; Columbia Township (MO); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Competitive compensation

401(k) with Company match

Career advancement pathway

Short- and Long-Term Disability

Health Savings and Flexible Spending

Health, Dental and Vision insurance

Generous PTO

Adoption Assistance

Paid Holidays

Wide selection of voluntary benefits

Job summary

ObjectiveHealth is seeking a Clinical Research Site Director in a full-time capacity to lead clinical trial activities at our site. The role requires strong leadership, patient interaction, and direct patient care, including consent, physical assessments, and coordinating IRB-approved protocols.

The ideal candidate will drive enrollment, ensure compliance with regulatory standards, and manage site visits while collaborating with investigators, sponsors, and monitors.

Qualifications

• Qualified for site leadership in clinical trials.
• 5+ years coordinating industry-sponsored trials.
• Experience with IRB-approved protocols.
• Ability to consent patients and perform basic clinical tasks.

Responsibilities

• Take ownership of assigned studies and patients.
• Communicate promptly with leadership and coworkers when issues arise.
• Maintain punctuality and reliability in scheduling and visits.
• Ensure strict regulatory compliance and data integrity across sites.
• Learn and use provided technologies to enhance daily activities.
• Uphold company values: Compassion, Integrity, Collaboration, Innovation, Velocity, Dedication.

Skills

Patient interaction

Team player

Leadership

IRB protocol

Clinical trial coordination

Patient care

Regulatory compliance

Communication

Advocacy

Focus under pressure

AE/SAE tracking

Therapy development domains

Job description

ObjectiveHealth is seeking a Clinical Research Site Director in a full-time capacity to lead clinical trial activities at our site. The role requires strong leadership, patient interaction, and direct patient care, including consent, physical assessments, and coordinating IRB-approved protocols.

The ideal candidate will drive enrollment, ensure compliance with regulatory standards, and manage site visits while collaborating with investigators, sponsors, and monitors.