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Posted Apr 21Research Assistant - Brunswick, OH
Brunswick, United StatesOn-site
Responsibilities
- Perform quality work within deadlines with or without direct supervision
Requirements
- By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Research Assistant
- By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite 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.
- The Iterative Health Site Network is a premier network of 70+ clinical research sites across US and Europe accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies.
- Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services.
- The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies.
- 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