Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)
Come Join Our Growing Team!
Paradigm Clinical Research is looking for clinical research staff to join our growing research team.
Clinical Research Assistant
We are looking for clinical research staff to join our dynamic research team! In this position you will provide exceptional customer service to patients participating in our clinical research studies.
At Paradigm Clinical Research, we provide high-quality care to our patients and high-quality data to our pharmaceutical sponsors! We are currently working on a variety of studies spanning many indications across a growing number of therapeutic areas daily.
Research staff are expected to:
Develop strong working relationships and maintain effective communication with study team members.
Adhere to an IRB-approved protocols.
Conduct telephone screenings: in person screenings to recruit potential subjects.
Collect and record study data. Input all information into database.
Assist and leads in activities related to clinical research studies including but not limited to answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires, patient medication dosing, temperature tracking and accountably, scheduling visits, data entry, patient visit prep, filing, organizing, rooming patients, participate in recruitment efforts, and more.
Maintain source documents and subject files in accordance with company procedures. Ensures accurate and complete compilation of subject data through chart reviews.
Follow all FDA, Good Clinical Practice (GCP) and ICH guidelines.
Job Type: Part-time
Pay: $23.00 - $25.00 per hour
Schedule:
Ability to Relocate:
Work Location: In person
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