Clinical Research Director directs and oversees the clinical research function for a healthcare organization. Develops research studies and creates standards and guidelines for clinical research services and programs. Being a Clinical Research Director ensures adherence to standard operating procedures, good clinical practice and FDA regulations. Requires an advanced degree. Additionally, Clinical Research Director typically reports to top management. The Clinical Research Director manages a departmental sub-function within a broader departmental function. Creates functional strategies and specific objectives for the sub-function and develops budgets/policies/procedures to support the functional infrastructure. Deep knowledge of the managed sub-function and solid knowledge of the overall departmental function. To be a Clinical Research Director typically requires 5+ years of managerial 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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