Clinical Trial Coordinator II - FSP

📋 Description

• Coordinate assigned clinical trial activities per plans, timelines, and quality standards.
• Review and document departmental, country, investigator, and study file materials; support audit
• Manage trial docs, eTMF reviews, and related communications/materials.
• Support site activation/start-up and regulatory submissions; track issues and resolutions.
• Maintain study trackers, training records, and system access across project teams.
• Collaborate with Global Investigator Services and stakeholders to resolve queries.

🎯 Requirements

• Bachelor’s degree preferred, with experience in clinical research or life sciences.
• At least 2 years in a Clinical Trial Coordinator or similar role.
• Hands-on experience with Veeva eTMF and CTMS is required.
• Experience coordinating global trials and vendor management preferred.
• Knowledge of ICH GCP, regulatory requirements, and clinical trial systems.
• Strong organizational, communication, and multi-tasking skills; attention to detail.

🎁 Benefits

• Fully remote: Work remotely from India in a global clinical research environment.
• Full-time position: Standard Monday-to-Friday schedule.
• Global exposure: Collaborate with international teams, investigators, sites, vendors, and
• Professional development: Grow across clinical trial coordination, site activation, feasibility
• Learning opportunities: Exposure to clinical trial technologies, systems, processes, and best
• Career growth: Take on additional responsibilities and contribute to process improvements.