Clinical Research Specialist, I-CARE 2 Study
2 days ago
The I-CARE 2 study is a randomized clinical trial that tests the impact of telehealth technology on informal caregivers and patients living with Alzheimer's disease and related dementias. As a Clinical Research Specialist, you will assist with identifying and recruiting potential research study subjects, determining eligibility, and coordinating study procedures.
Responsibilities- Conduct study visit activities, coordinate screening, consenting, and scheduling of tests, exams, and/or non-medical/behavioral interventions and assessments involving study subjects.
- Record study data, samples, and/or results in various databases, maintain databases for subjects and subject scheduling, and perform data validation checks.
- Monitor study team compliance with protocol and SOPs, submit regulatory paperwork, and communicate with PI and sub-investigators about concerns or recommended changes in study protocols.
- Assist with developing communications and strategies for advertising and recruitment, as well as developing information materials for study participants.
- Stay up-to-date on regulatory affairs and/or clinical research best practices by attending continuing education classes, conferences, seminars, and project team meetings.
Combinations of related education and experience may be considered. Education beyond the minimum required may be substituted for work experience. Work experience beyond the minimum required may be substituted for education.
- Bachelor's degree in science or a health-related field and 1 year of health-related or research experience; OR
- Associate's degree in an allied health profession and 3 years of health-related or research experience
The role regularly requires the ability to effectively communicate. The role frequently requires the ability to move about the work environment and to position oneself to operate laboratory equipment effectively.
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