IQVIA is looking to solve the problem of conducting clinical trial activities in accordance with all applicable regulations governing the conduct of clinical trials.
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.
- Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.
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.
- Assist in the informed consent process of research subjects.
Other
- Equivalent education and experience: a minimum of an associate’s degree.
- At least 1 year experience working in a clinical research setting preferred.
- Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.
- Develop strong working relationships and maintain effective communication with study team members.
- Please note, this position is not eligible for sponsorship.
