Sr Clinical Research Associate iProcess Global Research Inc

2.0 - 6.0 years

0 Lacs

karnataka

On-site

In this role at iProcess, you will be responsible for overseeing biospecimen collection studies across multiple countries. Your key responsibilities will include: - Serving as the primary point of contact for iProcess at specimen collection sites to ensure smooth communication and accurate clinical data transfer. - Facilitating Investigator and Sponsor Meetings, and actively participating in internal and external project meetings. - Managing regulatory documentation for study initiation, monitoring, and evaluation, including obtaining necessary approvals. - Drafting Collection Protocols, Consent Forms, and Case Report Forms (CRFs). - Independently conducting all types of monitoring visits (p...

Posted 1 week ago

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Senior Quality Auditor Precision Medicine Group

4.0 - 8.0 years

0 Lacs

karnataka

On-site

As a Senior Quality Auditor at Precision, you will play a crucial role in ensuring compliance with regulations and company procedures for clinical projects. Your responsibilities will include: - Supporting the Quality Management System by managing SOPs, training, and CAPA - Processing and maintaining documentation for controlled documents - Developing and administering training for employees and consultants - Hosting client/sponsor audits and supporting regulatory inspections - Coordinating and conducting assessments of vendors, including vendor audits - Conducting internal audits of quality systems, investigator site audits, and trial master file audits - Participating in computer systems v...

Posted 1 month ago

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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 months 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 2 months 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 3 months ago

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