IQVIA is looking to solve the problem of conducting clinical trial activities in accordance with applicable regulations, and is seeking an individual to assist in this process.
Requirements
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
- Medical Terminology knowledge preferred
- Clinical Skills preferred
- Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint)
- Demonstrated proficiency with clinical trial master filing systems
- Strong interpersonal skills with attention to detail
- Ability to prioritize and adapt quickly to changing business conditions
Responsibilities
- Assist with the screening, recruiting and enrollment of research subjects
- Perform patient/research participant scheduling
- Collect patient/research participant history
- Data entry and Management
- Coordinate follow-up care and laboratory procedures
- Adhere to an IRB approved protocol
- Assist in the informed consent process of research subjects
Other
- Develop strong working relationships and maintain effective communication with study team members
- Develop strong working relationships with the investigators and office staff
- Support the safety of research subjects
- Comply with Avacare, and Sponsor policies, standard operating procedures (SOPs) and guidelines
- Bachelor's degree not explicitly required but implied as a general requirement for the company
