Site Clinical Research Lead – Nephrology Trials

Panoramic Health; Saint Joseph (MI); On-site; USD 65,000 - 86,000; Full time

Job summary

Lake Michigan Nephrology in St. Joseph, MI is seeking a Clinical Research Coordinator II to lead site-level trial activities, from recruitment through study completion, ensuring patient safety, data integrity, and GCP compliance.

You’ll work with physicians, sponsors, and centralized teams to optimize recruitment workflows, manage study documentation, and coordinate visits, with a focus on accurate data capture and timely execution.

Qualifications

• 3–5+ years of clinical research experience.
• Bachelor’s degree in a health-related field preferred.
• GCP/IATA/ACRP or SOCRA certifications preferred.

Responsibilities

• Lead day-to-day clinical research activities at the site level across assigned clinical trials.
• Read and implement study protocols, including eligibility criteria and visit schedules.
• Prescreen patients and identify potential participants with clinic staff.
• Develop workflows to support recruitment, consent, enrollment, and retention.
• Coordinate with Central Enrollment Team to achieve enrollment goals.
• Obtain and document informed consent per protocol and SOPs.
• Train site staff on study objectives and maintain training records.
• Ensure space, equipment, and staffing meet study requirements.
• Coordinate protocol-specific visits and maintain compliant data collection.
• Collect, process, and ship laboratory specimens as required.
• Maintain source docs and study files; prepare for monitoring visits.

Skills

Clinical research

Bilingual English/Spanish

Communication skills

Attention to detail

Education

Bachelor’s degree in health-related field

Medical Assistant certification

GCP certification

IATA certification

ACRP certification

SOCRA certification

Job description

Lake Michigan Nephrology in St. Joseph, MI is seeking a Clinical Research Coordinator II to lead site-level trial activities, from recruitment through study completion, ensuring patient safety, data integrity, and GCP compliance.

You’ll work with physicians, sponsors, and centralized teams to optimize recruitment workflows, manage study documentation, and coordinate visits, with a focus on accurate data capture and timely execution.