Responsibilities
- Manage daily remote operations for clinical trials while following study protocols and regulatory standards.
- Facilitate virtual patient visits by coordinating appointments, maintaining records, and conducting follow-ups.
- Support recruitment efforts by assessing patient eligibility and qualifying candidates over the phone.
- Enter and update trial data accurately in electronic data capture and clinical trial management systems, resolving queries as needed.
- Help manage regulatory documents and submit or update materials for remote institutional review board approvals.
- Prepare for and engage in virtual monitoring sessions, audits, and inspections conducted by sponsors or contract research organizations.
- Act as a remote point of contact between sponsors, CROs, and internal research teams.
- Assist with initiating and closing studies, including gathering and verifying required documentation remotely.
- Track patient visit schedules and confirm all related documentation remains current and complete.
Benefits
- Be part of an organization dedicated to advancing clinical research through innovation.
- Operate fully remotely with opportunities to collaborate with a global team.
- Gain experience with diverse research protocols and emerging research methodologies.
- Access opportunities for professional growth and skill development.
- Work within a collaborative, respectful, and inclusive team environment.
Work Arrangement
Remote (Worldwide) — Mexico, Remote – U.S. Time Zones
Work Schedule
Full-time remote position requiring availability during U.S. time zones from EST to PST
Language Requirements
Fluent English communication, both spoken and written, is required
Additional Information
Bilingual skills are considered an advantage
