2. Utilizing Good Clinical Practice, the CRA ensures assigned study responsibilities are conducted in accordance with IRB and regulatory agency regulations.

3. Ensures site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities.

4. Completes timely and accurate data collection, documentation, entry, and reporting in both sponsor and ACH databases.

5. Participates with the PI in scientific writing, preparation of research abstracts, manuscripts, presentations for academic audiences and grant applications.

6. Specimen transporting, handling, processing, and shipping while maintaining correct records of specimen management and transport coordination according to protocol.

7. Collaborates with multidisciplinary teams across the enterprise. Participates in team meetings and discussions to provide updates on project status and contribute to research strategic planning.

8. Other duties as required.

Knowledge of clinical trial protocols is preferred.

2. Competency in interpreting medical charts and abstracting data is preferred

3. Knowledge of GCP, federal, state, and local regulations, including HIPAA policies and procedures.

Competency in the use of Microsoft Office, Word, and Excel, Electronic Health Systems, EPIC and databases utilized in research or have a

willingness to learn and demonstrate proficiency within six months of hire

Education and Experience

1. Education: : Bachelor's degree or bachelor's eligible in a relevant field (e.g. Biology, Heath Sciences, Data Science, Public Health, etc.) is required

2. Spanish speaking or Nepali speaking required

3. Certification: CITI Certification - Certification is required within 90 days of hire.

4. Years of relevant experience: none. Experience in research is preferred.