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Posted 3 hours agoResearch Assistant - Flowood, MS
Flowood, United StatesOn-site
Responsibilities
- Perform quality work within deadlines with or without direct supervision
Requirements
- By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need.
- High school diploma or equivalent. Some college preferred
- Ability to read, interpret, and apply clinic policies and research protocols
- Ability to use standard office software
- Must be able to lift up to 25 pounds
Contact
- experience more accessible to you, please contact CandidateAccommodations@iterative.health.
Additional details
- Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.
- We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology.
- Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.
- The RA is a specialized research professional working with and under the direction of the Clinical Principal Investigator (PI) and site management.
- The primary responsibility of the RA is to assist the Clinical Research Coordinators with conduct of research studies.
- The RA supports and facilitates the daily clinical trial activities and plays a supportive role in the conduct of the study. Responsibilities
- requirements to all individuals involved in the study
- Works with the Study Team to develop and implement recruitment strategies in accordance with site policies and IRB requirements and approvals
- Assists Study Team with screening subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion
- Assists Study Team as requested to register participants in the Clinical Trial Management System to ensure billing of study procedures to appropriate funding source