On-Site Clinical Trial Coordinator - Growth & Impact

Profound Research; Detroit (MI); On-site; USD 45,000 - 52,000; Full time

Benefits offered by this job

Full Benefits Package

Professional development support

On-site role

Job summary

Profound Research is seeking a Clinical Research Coordinator to manage trial activities on-site in Detroit, ensuring compliance with protocol, laws, and company standards.

You will train staff, oversee start-up, recruitment, data collection, regulatory documents, and safety reporting while maintaining high quality and ethics across all studies. Travel to partner sites may be required.

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 CCRC certification within 6 months of being in the role
• Experience performing clinical assessments, including vital signs, EKGs, blood draws, processing/shipping lab specimens

Responsibilities

• Conduct and manage all clinical trial activities in accordance with established research protocols and standards
• Complete all required training including ICH-GCP and IATA certification
• Mentor and train staff in clinical trials and trial management
• Lead duties for assigned trials including start up, vendor management, recruitment, data collection, and adverse event reporting
• Ensure good documentation practices across all trial records
• Communicate effectively with coworkers, leadership, sponsors, CROs, and vendors
• Collect and account for supplies from sponsors
• Other duties as assigned

Skills

Attention to detail

Team player

Independent worker

Education

Bachelor's degree in life sciences

Associate's degree + 4 years relevant experience

High School diploma + 6 years relevant experience

Job description

Profound Research is seeking a Clinical Research Coordinator to manage trial activities on-site in Detroit, ensuring compliance with protocol, laws, and company standards.

You will train staff, oversee start-up, recruitment, data collection, regulatory documents, and safety reporting while maintaining high quality and ethics across all studies. Travel to partner sites may be required.