Clinical Trials Compliance Specialist

Key responsibilities include creating eCRF specifications, design, development and validation of clinical trial setup process.Edit check specifications are created and setup at the trial levelUAT scripts are implemented to test the setup of the clinical studyDifferent instances of study URL(eg: UAT, production, testing etc.,) are set upUser accounts for...

Job DescriptionWe are seeking a diligent Clinical Site Auditor to ensure compliance and quality at Clinical Trial sites. You will conduct site audits, review documentation, and verify adherence to protocols, GCP, GLP, and regulatory requirements.As a seasoned auditor, you will be responsible for conducting thorough site audits, reviewing clinical research...

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