IQVIA is looking to solve the problem of conducting clinical trial activities in accordance with 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
- 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
- High School Diploma and 1 years’ relevant work experience in clinical research
- 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
- Equivalent education and experience
- Please note, this position is not eligible for sponsorship
