Clinical Secretary

Mcura Mobile Health; Gurugram District; On-site; INR 600,000 - 900,000; Full time

Job summary

Mcura Mobile Health is seeking a Clinical Trials Coordinator to coordinate and manage trials across regulatory and company standards. You will build and refine trial management systems to improve efficiency, while working with medical professionals, researchers, and staff to meet project milestones.

The role emphasizes data-driven decisions, site monitoring, and thorough documentation of protocols and forms, with collaboration across teams to ensure successful trial outcomes.

Responsibilities

• Coordinate and manage clinical trials, ensuring compliance with regulatory requirements and company standards.
• Develop and implement effective clinical trial management systems to enhance efficiency and productivity.
• Collaborate with cross-functional teams, including medical professionals, researchers, and administrative staff, to achieve project goals.
• Conduct site visits to monitor clinical trials, identify issues, and provide guidance to investigators.
• Analyze data from clinical trials to identify trends, risks, and areas for improvement, and develop reports to communicate findings to stakeholders.
• Ensure accurate and timely documentation of clinical trial activities, including protocols, case report forms, and investigational reports.

Job description

• Coordinate and manage clinical trials, ensuring compliance with regulatory requirements and company standards.
• Develop and implement effective clinical trial management systems to enhance efficiency and productivity.
• Collaborate with cross-functional teams, including medical professionals, researchers, and administrative staff, to achieve project goals.
• Conduct site visits to monitor clinical trials, identify issues, and provide guidance to investigators.
• Analyze data from clinical trials to identify trends, risks, and areas for improvement, and develop reports to communicate findings to stakeholders.
• Ensure accurate and timely documentation of clinical trial activities, including protocols, case report forms, and investigational reports.

Disclaimer: This job posting and Location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.