Clinical Research Coordinator — On-site Trials & Growth

Profoundresearch; Munster (IN); On-site; USD 60,000 - 90,000; Full time

Job summary

Profound Research in Munster, IN is seeking a Clinical Research Coordinator to manage trial activities under supervision, ensuring compliance with ICH-GCP and study protocols while upholding the company’s mission and values.

You will train staff, coordinate trial duties, manage source documents, and communicate with sponsors, CROs, and vendors; this is an on-site role with daily site visits and a focus on data integrity and patient safety.

Qualifications

• Bachelor’s degree with 2 years relevant life science experience OR
• Associate’s degree with 4 years relevant experience OR
• High School + 6 years relevant experience and 1 year CRC experience

Responsibilities

• Conduct and manage all clinical trial activities per protocols, in compliance with laws and procedures.
• Complete Profound Research required training including ICH-GCP and IATA in a timely manner.
• Mentor and train staff in trial conduct and management skills.
• Coordinate duties for assigned trials including start up, vendor management, subject recruitment, data collection, adverse event reporting, and visits.
• Ensure good documentation practices across source data, CRFs, queries, and regulatory forms.
• Communicate effectively with coworkers, leadership, sponsors, CROs, and vendors.
• Collect and account for supplies from sponsors.
• Other duties as assigned.

Skills

Attention to detail

Organization

Communication

Independent work

Team player

Education

Bachelor's degree with 2 years experience

Associate's degree with 4 years

High school diploma + 6 years experience

Job description

Profound Research in Munster, IN is seeking a Clinical Research Coordinator to manage trial activities under supervision, ensuring compliance with ICH-GCP and study protocols while upholding the company’s mission and values.

You will train staff, coordinate trial duties, manage source documents, and communicate with sponsors, CROs, and vendors; this is an on-site role with daily site visits and a focus on data integrity and patient safety.