PS Study Coordinator

About This Role

The Clinical Research Coordinator will coordinate technical and administrative details involved in clinical research studies to advance the understanding and improve care for patients with gastrointestinal diseases. This role supports the Microbiota and GI Immunology Consortia (MAGIC) Biobank by obtaining patient biospecimens, maintaining the biorepository, and asking clinically and scientifically relevant questions.

Responsibilities

• Attend and participate in Investigator and staff meetings, advising the team on study assignments and timelines.
• Carry out patient-facing functions including recruitment, screening, enrollment, and monitoring patient safety.
• Explain and obtain informed consent, medical history, and demographics from patients.
• Document and maintain historical data, status reports, and progress notes.
• Report and track adverse events, document protocol deviations, and prepare summary reports.
• Complete, audit, and correct case report forms.
• Maintain documents as required by FDA guidelines.
• Make statistical calculations, analyze data, and prepare reports summarizing results.
• Improve and document workflow quality and organization.
• Maintain contact with the IRB and prepare and submit IRB documents.

Requirements

• Bachelor's degree or equivalency
• IRB CITI Course in the Protection of Human Research subjects certificate within six months of hire
• Demonstrated human relations and effective communication skills
• Immunization according to CDC standards and hospital policy for patient-sensitive roles

Qualifications

• Bachelor’s degree in a related field, or equivalency (one year of education can be substituted for two years of related work experience)

Skills

* Required skills

Benefits

Certifications