Theranostics Clinical Trials Associate

BAMF Health, Inc.; Grand Rapids (MI); On-site; USD 42,000 - 60,000; Full time

Benefits offered by this job

Health plan with HSA

Flexible vacation time

401(k) retirement plan

Dental, vision, life insurance

Free downtown parking

Job summary

BAMF Health seeks a Clinical Trials Research Assistant to support study conduct, data collection, and patient scheduling at our Grand Rapids HQ. The role requires knowledge of GCP, good problem solving, and collaboration with the clinical research team to ensure study integrity.

Responsibilities include assisting with visits, biospecimen handling, data entry, and coordinating with coordinators and providers. A strong team environment and adherence to safety and regulatory standards are required.

Qualifications

• High school diploma required; GCP/IATA certifications preferred or required within 30 days.
• Experience with clinical trials processes and data management is a plus.
• Prior experience supporting study activities and coordinating scheduling.

Responsibilities

• Support clinical research team in study conduct and activities.
• Assist with scheduling, orders, and visits across EMR systems.
• Recruit subjects, collect data, and help organize research projects.
• Coordinate data entry and quality checks in protocol systems.
• Maintain compliance with GCP, federal and local regulations.
• Assist in communicating with providers, departments, and patients.
• Perform other duties as assigned by the research team.

Skills

Healthcare knowledge

GCP knowledge

Problem solving

Education

High School Diploma or GED

GCP Certification within 30 Days of hire

IATA Certification within 30 Days of hire

Shipping and Handling of Specimen Training

Job description

BAMF Health seeks a Clinical Trials Research Assistant to support study conduct, data collection, and patient scheduling at our Grand Rapids HQ. The role requires knowledge of GCP, good problem solving, and collaboration with the clinical research team to ensure study integrity.

Responsibilities include assisting with visits, biospecimen handling, data entry, and coordinating with coordinators and providers. A strong team environment and adherence to safety and regulatory standards are required.