Responsibilities
- Identify and onboard study participants remotely through digital marketing, referrals, online networks, and virtual engagement strategies.
- Lead virtual informed consent sessions and oversee electronic consent processes to confirm comprehension of study protocols, potential risks, and participant rights.
- Manage all aspects of remote study operations, including telehealth appointments, digital assessments, shipping of biological samples via external partners, and continuous virtual monitoring.
- Gather and manage clinical data and real-world evidence collected through digital systems, such as uploaded medical records, electronic patient-reported outcomes, and digital inputs.
- Track protocol compliance and scheduled visits using remote monitoring tools; record adverse events and concurrent medications from participant submissions and documentation.
- Ensure thorough and up-to-date electronic records, including source documentation, case report forms, and digital regulatory files.
- Assist with IRB applications, modifications, and renewal requests using remotely maintained records, summaries, and participant communications.
- Work with data, product, and operations teams through virtual collaboration to resolve issues in decentralized workflows and uphold data integrity.
Work Arrangement
Remote (Worldwide)
