Field Research Assistant: Biomarkers & Data

Rosalind Franklin University of Medicine & Science; North Chicago (IL); Vor Ort; USD 30.000 - 33.000; Vollzeit

Benefits dieser Stelle

Medical coverage

Dental coverage

Vision coverage

Paid parental leave

Disability insurance

Life insurance

401(k)/403(b) with employer match

Vacation and holidays

Zusammenfassung

Rosalind Franklin University of Medicine and Science (RFUMS) in North Chicago, IL seeks a full-time Research Assistant for a DoD-funded project on urinary proteomic biomarkers of bone adaptation. You will support field data collection, biospecimen handling, and study logistics across sites with travel to field locations as needed.

Under supervision, you will ensure protocol compliance, data quality, and regulatory adherence, while coordinating IRB processes and participant scheduling for a

Qualifikationen

• Relevant health/biological science background and clinical research exposure.
• Experience following SOPs, study protocols, and regulatory requirements.
• Record-keeping and data integrity emphasis.

Aufgaben

• Coordinate participant logistics across study timepoints and sites.
• Support IRB-approved recruitment, consent, screening, and participant relations.
• Perform field data collection and biospecimen handling per SOPs.
• Maintain study records, data quality checks, and regulatory compliance.
• Manage equipment, inventories, and sample transport across sites.
• Assist with progress reporting and dissemination activities.

Kenntnisse

Strong organization

Attention to detail

Clear communication

Data management

Ability to work independently

Team collaboration

Ausbildung

Master's degree in biological sciences or related field

Bachelor's degree in health sciences or related field

Jobbeschreibung

Rosalind Franklin University of Medicine and Science (RFUMS) in North Chicago, IL seeks a full-time Research Assistant for a DoD-funded project on urinary proteomic biomarkers of bone adaptation. You will support field data collection, biospecimen handling, and study logistics across sites with travel to field locations as needed.

Under supervision, you will ensure protocol compliance, data quality, and regulatory adherence, while coordinating IRB processes and participant scheduling for a