IQVIA is looking to hire a Research Assistant to help conduct clinical trial activities in accordance with all applicable regulations.
Requirements
- Working knowledge of clinical trials.
- Working knowledge of the principles of Good Clinical Practices (GCP).
- In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
- Skill in carrying out required clinical procedures.
- Working knowledge of medical terminology.
- Ability to pay close attention to detail.
- Equivalent education and experience - High School Diploma and 1 years’ relevant work experience in clinical research.
Responsibilities
- EDC Entry and Query Resolution
- Assist with the screening, recruiting, and enrollment of research subjects.
- Perform patient/research participant scheduling.
- Collect patient/research participant history.
- Coordinate follow-up care and laboratory procedures.
- Adhere to an IRB-approved protocol.
- Coordinate protocol-related research procedures, study visits, and follow-up care.
Other
- Develop strong working relationships and maintain effective communication with study team members.
- Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office.
- Assist in the informed consent process of research subjects.
- Support the safety of research subjects.
- Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.
