Clinical Trial Coordinator — Patient-Centric Research

Profoundresearch; Detroit (MI); On-site; USD 55,000 - 75,000; Full time

Job summary

Profound Research invites applications for a Clinical Research Coordinator to manage trial activities on-site with physicians guiding the patient-centric research model. You will coordinate study startup, recruitment, data collection, and regulatory documentation, ensuring strict adherence to ICH-GCP and company procedures.

The role requires relevant life sciences experience, strong attention to detail, and effective communication with diverse stakeholders.

Qualifications

• Bachelor’s degree or higher in life sciences with required experience
• Associate’s degree with 4+ years of life science experience
• High School/technical degree with 6+ years life science experience
• Clinical Research Coordinator experience
• GCP certification and CCRC certification within 6 months of hire

Responsibilities

• Conduct and manage all clinical trial activities per protocol and regulations
• Complete required Profound Research training including ICH-GCP and IATA certifications
• Mentor and train staff on trial conduct and management
• Lead study startup, vendor management, subject recruitment, and data collection
• Ensure good documentation practices across study records and forms
• Communicate professionally with investigators, sponsors, CROs and vendors
• Handle supplies and regulatory documents for trials
• Perform other duties as assigned

Skills

GCP certification

CCRC certification

Clinical assessments

Communication

Team player

Attention to detail

Education

Bachelor’s degree in life sciences

Associate’s degree + 4 years relevant life science experience

High School diploma/technical degree + 6 years life science experience

Clinical Research Coordinator experience

Job description

Profound Research invites applications for a Clinical Research Coordinator to manage trial activities on-site with physicians guiding the patient-centric research model. You will coordinate study startup, recruitment, data collection, and regulatory documentation, ensuring strict adherence to ICH-GCP and company procedures.

The role requires relevant life sciences experience, strong attention to detail, and effective communication with diverse stakeholders.