Assistant Clinical Research Associate (Remote)

About the role

Join a global team supporting leading pharmaceutical and biotech companies in delivering clinical trials across more than 100 countries. As an Assistant Clinical Research Associate you will work remotely on assigned projects, supporting site preparedness, logistics, and monitoring activities in line with SOPs and regulatory guidelines.

Key responsibilities

• Perform site‑preparation tasks, including pre‑study assessments and waiver support.
• Customize Site ICFs with site contact details and review patient‑facing materials.
• Conduct remote EMR/EHR checklist reviews and verify document collection status.
• Coordinate system access for site staff, track vendor qualifications, and manage study supplies.
• Support essential document collection, updates in company systems, and site payment processes.
• Execute reconciliation tasks for CRFs, queries, deviations, SAEs, and safety reports.
• Maintain vendor trackers and assist with centralized monitoring tools.
• Follow up on missing or expired documents and drive corrective actions.

Required profile

• Strong attention to detail and ability to follow SOPs and regulatory guidelines.
• Excellent organizational skills for managing multiple site activities.
• Effective communication with CRA, study leads, and site staff.

Required skills

• Experience with EMR/EHR systems.
• Familiarity with CRF and query management.
• Understanding of SOPs and clinical trial documentation processes.

What we offer

• Opportunity to work on high‑impact clinical trials for top pharma and biotech firms.
• Remote work flexibility within a standard Monday‑Friday schedule.
• Professional development in clinical research operations.