Clinical Research Coordinator - Lead Trials On-Site

Profound Research LLC; Detroit, Northern (MI, KY); Hybrid; USD 60,000 - 80,000; Full time

Benefits offered by this job

Meaningful impact

Professional growth

Leadership opportunities

Collaborative culture

Full benefits

Job summary

Profound Research LLC is seeking a Clinical Research Coordinator to manage trial activities under supervision, ensuring compliance with protocol, laws, and company values. You will coordinate site activities, train staff, and maintain high-quality study documentation.

The role requires a Bachelor’s or equivalent, with 2+ years in life sciences, and certification in GCP/CCRC within six months. On-site work with daily site commutes is expected, supporting multiple trial sites.

Qualifications

• Bachelor’s degree and 2 years relevant experience in the life science industry OR
• Associate’s degree with 4 years relevant experience in the life science industry OR
• High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year
• Clinical Research Coordinator experience
• Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role
• Experience performing clinical assessments, including vital signs, EKGs, blood draws, processing/shipping lab specimens
• Proficient ability to work independently, plan and prioritize with minimal guidance
• Excellent attention to detail, organization, and communication with varied stakeholders
• Ability to work as a team player with the ability to adapt to changing schedules and assignments

Responsibilities

• Conduct and manage all clinical trial activities in accordance with established research protocols and standards.
• Complete all required Profound Research training, including ICH-GCP and IATA certifications.
• Mentor and train staff in trial conduct, protocol requirements, communication and trial management.
• Lead, implement and coordinate duties for assigned trials including start up, vendor management, recruitment, regulatory documents and data collection.
• Ensure good documentation practices across study data and records.
• Communicate effectively with coworkers, leadership, subjects, sponsors, CROs and vendors.
• Collect and account for supplies from sponsors such as lab kits and investigational products.
• Other duties as assigned.

Skills

Attention to detail

Organization

Communication with stakeholders

Team player

Adaptability

Education

Bachelor’s degree

Associate’s degree

High School Diploma

Tools

GCP certification

CCRC certification

Job description

Profound Research LLC is seeking a Clinical Research Coordinator to manage trial activities under supervision, ensuring compliance with protocol, laws, and company values. You will coordinate site activities, train staff, and maintain high-quality study documentation.

The role requires a Bachelor’s or equivalent, with 2+ years in life sciences, and certification in GCP/CCRC within six months. On-site work with daily site commutes is expected, supporting multiple trial sites.