Regulatory Coordinator

Roles & Responsibilities
• Coordinate regulatory documentation for clinical research studies
• Prepare and submit regulatory documents to ethics committees and authorities
• Maintain essential study files and ensure compliance with regulatory guidelines
• Assist in study start-up activities and documentation management
• Ensure adherence to GCP and applicable regulatory standards
• Support communication between sponsors, investigators, and regulatory bodies

Qualification
• Pharm D Graduate
• Freshers can apply

Experience
• Freshers eligible
• Prior internship or exposure to clinical research preferred

Skills
• Knowledge of clinical research and regulatory processes
• Understanding of ICH-GCP guidelines
• Strong documentation and organizational skills
• Good communication skills
• Ability to work remotely and manage timelines effectively

About the Company
Koncord Clinical Research Services (KCRS) is a clinical research organization focused on delivering regulatory and research support services. The company provides opportunities for healthcare graduates to build careers in clinical research with exposure to regulatory coordination and study management activities.