Study Personnel

Liveon Biolabs Pvt. Ltd.

Tumakuru

On-site

INR 300,000 - 600,000

Full time

9 days ago
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Job summary

Liveon Biolabs Pvt. Ltd. in Tumakuru, India seeks a dedicated study coordinator to oversee study activities and ensure regulatory compliance. You will maintain accurate study records, collaborate with scientists, and monitor progress through site visits.

The role involves preparing essential documents, monitoring for protocol deviations, and promptly addressing study-related issues to support project timelines and data integrity.

Qualifications

  • Experience coordinating clinical or study activities.
  • Familiarity with regulatory requirements in research.
  • Strong record-keeping and documentation skills.

Responsibilities

  • Coordinate and manage study-related activities, ensuring compliance with regulatory requirements.
  • Develop and maintain accurate records of study data, including protocols, case report forms, and investigational reports.
  • Collaborate with cross-functional teams, including biologists, chemists, and statisticians, to achieve study objectives.
  • Conduct site visits to monitor study progress, identify issues, and implement corrective actions.
  • Prepare and review study documents, such as informed consent forms, case report forms, and study protocols.
  • Ensure timely resolution of study-related issues, including adverse events and protocol deviations.

Job description

  • Coordinate and manage study-related activities, ensuring compliance with regulatory requirements.
  • Develop and maintain accurate records of study data, including protocols, case report forms, and investigational reports.
  • Collaborate with cross-functional teams, including biologists, chemists, and statisticians, to achieve study objectives.
  • Conduct site visits to monitor study progress, identify issues, and implement corrective actions.
  • Prepare and review study documents, such as informed consent forms, case report forms, and study protocols.
  • Ensure timely resolution of study-related issues, including adverse events and protocol deviations.
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