FULLTIME
Study Personnel
Liveon Biolabs
Not specified · onsite · Posted 13d ago
Sourced from
Undisclosed0–3 yrsfulltimeNot specified
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Section · 01
About this role
- 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.
Disclaimer: This job posting 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.
Sourced from naukri
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Section · 02
Skills
site visitsclinical researchtraining programsgoogle cloud platformMicrosoft Office SuiteResearchCommunication Skillscompliance