Project Co-ordinator (Clinical Research)

Roles & Responsibilities
• Coordinate and oversee site-level clinical trial activities to ensure protocol compliance
• Support end-to-end clinical research operations including planning, execution, tracking, and reporting
• Act as a supervisory link between CRAs, site teams, and internal stakeholders
• Monitor project timelines, deliverables, and quality metrics across assigned studies
• Ensure compliance with ICH-GCP guidelines, SOPs, and applicable regulatory requirements
• Identify operational risks and support implementation of corrective and preventive actions (CAPA)
• Contribute to continuous quality improvement initiatives in clinical research operations

Qualification
• B.Pharm (Bachelor of Pharmacy), M.Pharm (Master of Pharmacy), Pharm.D (Doctor of Pharmacy), M.Sc, B.Sc, Life Sciences (related disciplines)

Experience
• 3-4 years of on-site experience as a Clinical Research Associate (CRA)
• 4-5 years of total experience in clinical research operations
• Minimum 2 years in a project management or supervisory role

Skills
• Strong knowledge of clinical trial operations and site management
• Sound understanding of ICH-GCP and regulatory requirements
• Leadership and team coordination skills
• Excellent organizational, communication, and problem-solving abilities
• Ability to manage multiple projects, timelines, and stakeholders effectively

About the Company
Hector Research & Archival Pvt. Ltd. is a clinical research organization committed to operational excellence and uncompromised quality in clinical trials, supporting site-level execution and regulatory compliance across India while driving high-quality clinical research outcomes.