Scientist - Clinical Research assumes lead role in various clinical research projects. Proposes, plans, organizes and executes experiments and research. Being a Scientist - Clinical Research secures grants and funding for research and is responsible for controlling budgets. Summarizes findings in reports and communicates results. Additionally, Scientist - Clinical Research interacts with other scientists within and outside of the organization. Provides recommendations that influence extensive clinical research activities. Requires an advanced degree. Typically reports to head of a unit/department. The Scientist - Clinical Research work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Scientist - Clinical Research typically requires 4 -7 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