Clinical Research Site Leader - Growth, Impact, Benefits

Profound Research; Hobart (IN); On-site; USD 75,000 - 95,000; Full time

Benefits offered by this job

Health insurance

PTO

Retirement plan

Professional development support

Job summary

Profound Research is seeking a seasoned Clinical Research Coordinator to oversee site activities and ensure compliance across trial protocols. You will supervise staff, coordinate enrollment, and liaise with sponsors, CROs, and physicians to optimize patient enrollment and study performance.

Join a mission-driven team committed to rigorous scientific standards, regulatory excellence, and patient-centered care in a growing network of research sites. Travel regionally as required.

Qualifications

• Associate degree or BS/BA in Life Sciences or related discipline.
• 8+ years prior experience as a clinical research coordinator
• 3-5 years of direct line management responsibilities
• Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification preferred.
• Experience performing clinical assessments, including vital signs, EKGs, blood draws, processing/shipping lab specimens.
• Demonstrated ability to foster concepts of teamwork, cooperation, self- control, and flexibility to get the work done.
• Excellent attention to detail, organization, and communication with varied stakeholders.
• Able to travel regionally and to professional meetings as required.

Responsibilities

• Maintain site compliance for all clinical trial activities per protocols and regulations.
• Maintain working knowledge of FDA regulations, ICH-GCP guidelines, SOPs, and study protocol(s).
• Supervise assigned site, conduct performance reviews, coaching, and disciplinary actions if needed.
• Ensure training of staff for compliance and inspection readiness.
• Collaborate with Operations and Business Development on feasibility and study placement.
• Oversee enrollment planning and success across studies; understand revenue expectations.
• Serve as primary CRC on at least one trial of medium to high complexity; train for continued qualifications.
• Share best practices with other Profound site locations to raise operational competencies.
• Coordinate with Quality Assurance to ensure site quality and CAPA processes.
• Build relationships with outside medical practices and hospitals to aid patient recruitment.
• Act as site liaison with coworkers, leadership, sponsors, CROs, and vendors.
• Meet weekly, monthly, and quarterly goals for the sites.
• Help build scalable operations infrastructure at new Profound sites as needed.
• Other duties as assigned by leadership.

Skills

Attention to detail

Communication

Teamwork

Flexibility

Education

Associate degree in Life Sciences

BS/BA in Life Sciences

Tools

GCP Certification

CCRC Certification

Job description

Profound Research is seeking a seasoned Clinical Research Coordinator to oversee site activities and ensure compliance across trial protocols. You will supervise staff, coordinate enrollment, and liaise with sponsors, CROs, and physicians to optimize patient enrollment and study performance.

Join a mission-driven team committed to rigorous scientific standards, regulatory excellence, and patient-centered care in a growing network of research sites. Travel regionally as required.