Sr Clinical Research Associate iProcess Global Research Inc

2.0 - 6.0 years

0 Lacs

karnataka

On-site

Role Overview As a Senior Clinical Research Associate (CRA) at iProcess, you will be responsible for overseeing biospecimen collection studies across multiple countries. Your main duties will include ensuring compliance with international regulations, maintaining biospecimen integrity, and enforcing adherence to study protocols. Acting as a key liaison between global clinical sites, biorepositories, laboratories, and internal teams, you will play a crucial role in supporting high-quality data and sample collection. Key Responsibilities - Serve as the primary point of contact for iProcess at specimen collection sites, ensuring smooth communication and accurate clinical data transfer. - Facili...

Posted 2 weeks ago

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Clinical Data Management Specialist SyMetric

2.0 - 6.0 years

0 Lacs

karnataka

On-site

Role Overview: You will be working as a Clinical Data Management Specialist at SyMetric in Bengaluru. Your main responsibilities will include tasks related to Clinical Data Management such as Study setup, UAT, Query Management, Study start-up, Conduct, and close-out phase. Key Responsibilities: - Perform Study setup activities - Conduct User Acceptance Testing (UAT) - Manage queries related to clinical data - Coordinate Study start-up and close-out phase Qualification Required: - Possess Clinical Data Management and Electronic Data Capture (EDC) skills - Previous experience in Project Management is preferred - Demonstrate excellent data management skills - Have familiarity with clinical data...

Posted 3 weeks ago

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Senior Quality Auditor Precision Medicine Group

4.0 - 8.0 years

0 Lacs

karnataka

On-site

The Senior Quality Auditor provides support to the audit program and clinical projects to ensure compliance with regulations and Precision procedures. You will be responsible for offering oversight and subject matter expertise to quality and compliance activities, aiding project teams throughout all phases of a clinical study. Your essential job functions will include supporting the Quality Management System by managing SOPs, training, and CAPA. You will be required to process and maintain documentation for controlled documents as needed. Additionally, you will develop and conduct training for employees and consultants. Hosting client/sponsor audits, supporting regulatory inspections, coordi...

Posted 1 month ago

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