Research Coordinator

- Experience coordinating clinical trials or investigator-initiated research studies.

- Project management skills.

- Knowledge and certification of Good Clinical Practice –ICH-GCP.

- Demonstrated knowledge of research ethics including research confidentiality and privacy.

- Proficiency in Microsoft Office applications (e.g., Outlook, Word, Excel).

- Experience with REDCap or other clinical research databases, including database setup, data entry and data quality checks.

- Ability to think analytically and conceptually.

- Ability to maintain accuracy and attention to detail.

- Ability to communicate effectively, both verbally and in writing.

- Highly effective interpersonal and organizational skills.

- Ability to multi-task and prioritize work to meet deadlines.

-Ability to work effectively independently and in a team environment.

-Demonstrated initiative and ability to follow through on tasks, coordinate follow-up and identify issues requiring the Principal Investigators' attention.