Senior Clinical Research Coordinator

Roles & Responsibilities:
• Strong knowledge of Clinical Research and patient recruitment processes
• Coordinate communication between physician, patient, and Site Head
• Conduct patient screening including informed consent, randomization, enrollment, and follow-ups (including telephonic follow-ups)
• Maintain Investigator Master File (IMF) as per Good Documentation Practices and SOPs, including source document generation
• Attend Site Initiation Visits, Monitoring Visits, and Close-Out Visits
• Perform CRF and e-CRF data entry and resolve data queries
• Coordinate with laboratories and manage shipment logistics
• Assist pharmacist in drug accountability and temperature log maintenance
• Support study material accountability and scheduling study procedures
• Prepare file notes and submit weekly/monthly reports
• Track study activities and report daily updates to Site Head

Qualification:
• MSc (Life Sciences)
• Pharm D
• M.Pharm

Experience:
• Minimum 2 years in Clinical Research (Freshers not eligible)

Skills:
• Knowledge of GCP and clinical trial processes
• Good communication skills (Gujarati, Hindi, English)
• Documentation and data management skills
• Strong coordination and organizational abilities

About the Organization:
The organization is engaged in clinical research activities in Ahmedabad, ensuring ethical trial conduct, regulatory compliance, and high standards of patient care. It provides structured clinical trial management and professional growth opportunities for research professionals.