Roles & Responsibilities:
• Coordinate and support site-level clinical trial operations.
• Act as a liaison between investigators, sponsors, CROs, and internal teams.
• Track study timelines, milestones, and deliverables to ensure on-time execution.
• Ensure compliance with ICH-GCP, SOPs, and applicable regulatory requirements.
• Support study start-up, ongoing trial management, and close-out activities.
• Maintain accurate and complete clinical trial documentation and reports.
• Assist in monitoring site performance and resolving operational challenges.
• Support audits, inspections, and quality improvement initiatives.
Qualification:
• Bachelor’s or Master’s degree in Life Sciences, Medical Sciences, Pharmacy, or related field.
Experience:
• 3–4 years of experience as a Project Coordinator or Project Manager in Clinical Research.
Skills:
• Strong understanding of clinical operations and site management.
• Excellent communication, coordination, and leadership skills.
• High attention to detail and strong organizational abilities.
• Ability to manage multiple activities and stakeholders effectively.
• Commitment to research quality, compliance, and ethical standards.
About the Organization:
The organization is a growing clinical research organization focused on delivering high-quality clinical trial execution through strong site-level operations and regulatory compliance. It offers professionals an opportunity to work in a dynamic environment, collaborate with cross-functional stakeholders, and contribute to impactful clinical research projects.
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