Research Assistant -Providence, RI

The role

The Research Assistant supports the day-to-day conduct of active clinical trials under the direction of the Principal Investigator and site management. This role assists Clinical Research Coordinators with participant screening, enrollment, documentation, data entry, and compliance.

What you will do

• Assist the Study Team with communicating study requirements to all individuals involved in the study.
• Work with the Study Team to develop and implement recruitment strategies.
• Assist with screening subjects for eligibility using protocol-specific inclusion and exclusion criteria.
• Assist with registering participants in the Clinical Trial Management System (CTMS).
• Collect and report ongoing patient recruitment and enrollment progress and metrics.
• Assist the Study Team in completing study documentation and maintaining study files.
• Enter all patient visit data in eCRF and CTMS on a daily basis or as directed.
• Arrange secure storage of study documents in accordance with GCP guidelines.
• Maintain inventory of study supplies.
• Process and ship specimens per study protocol and IATA regulations as directed.

Required qualifications

• High school diploma or equivalent
• Minimum 2 years of experience in a healthcare setting
• Strong written and verbal communication skills
• Ability to read, interpret, and apply clinic policies and research protocols
• Proficiency in standard office software
• Highly organized with the ability to manage multiple tasks and meet deadlines
• Ability to work both independently and collaboratively as part of a research team
• Professional, detail-oriented, and committed to maintaining confidentiality and data integrity
• Ability to sit, stand, and move throughout clinical and office environments for extended periods of time
• Ability to lift and move up to 25 pounds as needed

Nice to have

• some college coursework
• familiarity with CTMS or eCRF platforms
• Prior clinical research experience or exposure to clinical trial operations
• Familiarity with GCP guidelines and human subject research regulations
• Experience with specimen processing and shipping per IATA regulations
• Interest in pursuing a career path in clinical research coordination or research operations

About the company

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The company has a network of 100+ sites across the US, Europe, India, and Australia.