Contract Clinical Trials Coordinator

Profound Research LLC

Northern, Rochester (KY, MI)

Hybrid

USD 45,000 - 52,000

Full time

6 days ago
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Benefits offered by this job

Full Benefits Package
Professional Development Support

Job summary

Profound Research LLC is seeking a Clinical Research Coordinator to oversee trial activities at on-site sites in compliance with protocols, laws, and company values. You will train staff, coordinate start-up, recruitment, and data collection, and ensure proper documentation and regulatory compliance.

The role requires a bachelor’s degree in life sciences or equivalent with 2+ years of relevant experience, GCP certification, and strong attention to detail and communication skills.

Qualifications

  • Bachelor’s degree in life sciences or equivalent with relevant experience.
  • Associate’s degree plus 4 years life science experience acceptable.
  • High School/technical diploma with 6+ years life science experience acceptable.
  • Clinical Research Coordinator experience required.
  • Certification: GCP within 6 months of start.

Responsibilities

  • Manage clinical trial activities under supervision per protocol and regulations.
  • Complete required training including ICH-GCP and IATA as applicable.
  • Mentor staff on trial conduct, protocol requirements, and data handling.
  • Coordinate study start up, vendor management, and subject recruitment.
  • Ensure good documentation practices and accurate regulatory records.

Education

Bachelor’s degree in life sciences
Associate’s degree with 4 years life science experience
High School Diploma with 6 years life science experience
Clinical Research Coordinator experience
GCP certification
Strong attention to detail and communication

Job description

Profound Research LLC is seeking a Clinical Research Coordinator to oversee trial activities at on-site sites in compliance with protocols, laws, and company values. You will train staff, coordinate start-up, recruitment, and data collection, and ensure proper documentation and regulatory compliance.

The role requires a bachelor’s degree in life sciences or equivalent with 2+ years of relevant experience, GCP certification, and strong attention to detail and communication skills.

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