Irb Jobs in Emory, GA (NOW HIRING)

IRB USA Inspire Resources is seeking a skilled Data Scientist in Atlanta, Georgia, who will perform extensive analyses on various data sources to facilitate business decisions. The ideal candidate ...

The IRB Director also guides and educates faculty, staff, and IRB members on human subjects research compliance. Key Responsibilities * Oversight and Compliance * Direct all IRB operations to ensure ...

Position Information The IRB Director is responsible for providing strategic leadership, administrative management, and regulatory oversight of the Institutional Review Board at Morehouse School of ...

Prepare, submit, and maintain IRB applications, amendments, and continuing reviews. Retrieve and compile retrospective clinical and imaging data from the EPIC electronic health record system.

Ensure that study activities are conducted in accordance with GCP, IRB guidelines, and sponsor requirements. Maintain accurate and up-to-date source documentation and regulatory binders.

Ensure regulatory documentation and study activities meet FDA, ICH-GCP, HIPAA, IRB, sponsor, and organizational requirements * Conduct quality reviews, implement SOPs and CAPAs, and maintain audit ...

Ensure regulatory documentation and study activities meet FDA, ICH-GCP, HIPAA, IRB, sponsor, and organizational requirements * Conduct quality reviews, implement SOPs and CAPAs, and maintain audit ...

This role is responsible for assisting with regulatory submissions (IRB and IACUC), coordinating clinical study operations, and contributing to the preparation of scientific manuscripts and ...

Ensure compliance with IRB, FERPA, HIPAA (where applicable), GDPR, and funding agency requirements. * Lead risk management for sensitive, proprietary, and regulated data environments. * Operational ...

Research/Scholarship - 10% Complete CITI training, IRB training and obtaining IRB online access. Engage in clinical, translational, or basic science research relevant to OMFS. Publish scholarly work ...

This role is responsible for assisting with regulatory submissions (IRB and IACUC), coordinating clinical study operations, and contributing to the preparation of scientific manuscripts and ...

Ensure compliance with IRB, FERPA, HIPAA (where applicable), GDPR, and funding agency requirements. * Lead risk management for sensitive, proprietary, and regulated data environments. * Operational ...

This role is responsible for assisting with regulatory submissions (IRB and IACUC), coordinating clinical study operations, and contributing to the preparation of scientific manuscripts and ...

This role is responsible for assisting with regulatory submissions (IRB and IACUC), coordinating clinical study operations, and contributing to the preparation of scientific manuscripts and ...

This role is responsible for assisting with regulatory submissions (IRB and IACUC), coordinating clinical study operations, and contributing to the preparation of scientific manuscripts and ...

Scholarship - 10% Complete CITI training, IRB training and obtaining IRB online access. Engage in clinical, translational, or basic science research relevant to OMFS. Publish scholarly work in peer ...

Scholarship - 10% Complete CITI training, IRB training and obtaining IRB online access. Engage in clinical, translational, or basic science research relevant to OMFS. Publish scholarly work in peer ...

Ensure compliance with IRB, FERPA, HIPAA (where applicable), GDPR, and funding agency requirements. * Lead risk management for sensitive, proprietary, and regulated data environments. * Operational ...

Ensure compliance with IRB, FERPA, HIPAA (where applicable), GDPR, and funding agency requirements. * Lead risk management for sensitive, proprietary, and regulated data environments. * Operational ...

Demonstrates research processes and Institutional Review Board (IRB) rules. * Assists with navigation of research processes/research tracking for IRB application; offers feedback on writing research ...