Clinical Research Coordinator

Role Overview

This position involves managing and coordinating multiple clinical research activities across various healthcare settings within the Delhi-NCR region. The Coordinator will facilitate seamless clinical trial execution, ensure participant compliance, and maintain rigorous documentation and regulatory adherence.

Key Responsibilities

• Perform 3 to 4 site or field visits daily to hospitals, clinics, doctors, and research facilities to manage relationships and execute study processes.
• Oversee daily operations of clinical trials, ensuring all are conducted per established study protocols.
• Recruit suitable study participants by screening and enrolling them, ensuring all documentation is accurate and complete.
• Develop and manage participant lead generation by leveraging doctor referrals, promotional campaigns, and database outreach.
• Obtain informed consent from participants, clearly explaining study procedures, potential risks, and benefits.
• Ensure compliance with clinical trial protocols, standard operating procedures (SOPs), Good Clinical Practice (GCP) guidelines, and regulatory standards.
• Maintain thorough and current clinical study records, reports, and related documentation.
• Collaborate with investigators, doctors, and research teams to support the smooth execution of clinical studies.
• Conduct regular interactions with clinical sites and physicians to monitor patient recruitment and study progress.
• Oversee participant follow-ups, monitor their progress, and address any study-related issues efficiently.
• Assist with data collection, data entry, resolving queries, and maintaining data integrity.
• Prepare for audits and inspections by ensuring all compliance requirements and documentation are properly managed.
• Create reports and presentations regarding study progress and clinical outcomes for various stakeholders.
• Identify operational issues and coordinate solutions to facilitate timely completion of clinical trials.
• Maintain professional and respectful communication with patients, healthcare professionals, and external research collaborators.

Additional Information

This role demands dedication to compliance, strong interpersonal skills for stakeholder interaction, and rigorous attention to detail to safeguard data quality and patient safety.