Healthcare Fraud Investigator Employment Type: Full-Time, Mid-Level Department: Litigation Support CGS is seeking... a Healthcare Fraud Investigator to provide Legal Support for a large Government Project in Nashville, TN. The candidate...
reports *Assists with regulatory compliance guidance oversight of investigator initiated multi-center trials *Trains... and/or regulatory compliance in a research or clinical setting. *An equivalent combination of education and experience may...
supervision and training of regulatory staff, maintaining compliance with institutional and federal regulations, and supporting... gaps in compliance and implement corrective actions where needed· Prepares sponsor-required regulatory documents (site...
research billing review *Maintain an up-to-date regulatory binder *Schedule and attend sponsor visits; and prepare and submit... IRB paperwork to ensure compliance with IRB regulations *Incumbent may assist with grant or manuscript preparation...
study source documents Report adverse events Understand good clinical practice (GCP) and regulatory compliance Educate..., submit, and maintain essential regulatory documents (e.g. IRB, FDA, etc.) and remain aware of the regulatory status...
Nemours Philadelphia Thomas Jefferson University location by assisting in regulatory document preparation and collection... as required by sponsoring agencies; attends Investigator Meetings, as assigned Understands and can conduct clinical research studies...
to cultural resources. Provides regulatory compliance support for Federal, state, municipal, and commercial clients. Supports..., and prepare compliance reports. Responsibilities include, but are not limited to: Serves as a Senior Field Director...
, and data recovery efforts, analyze prehistoric and historic artifacts, and prepare compliance reports. Responsibilities... of the Principal Investigator including scheduling work and making individual or team work assignments and leading the...
, and data recovery efforts, analyze prehistoric and historic artifacts, and prepare compliance reports. Responsibilities... of the Principal Investigator including scheduling work and making individual or team work assignments and leading the...
, and investigator-initiated studies of gastrointestinal motility, gastrointestinal transit, and gastroparesis. In this capacity..., this person will work closely with the principal investigator on projects which will involve assessing gastrointestinal motility...
to cultural resources. Provides regulatory compliance support for Federal, state, municipal, and commercial clients. Supports..., and prepare compliance reports. Responsibilities include, but are not limited to: Serves as a Senior Field Director...
, effectively assign and monitor multiple tasks simultaneously, and work closely with their study Principal Investigator (PI... and/or other study related documentation Research Study Compliance Adhere to IRB approved protocols and compliance with HIPAA...
collection/entry. Manage regulatory binders, IRB submissions, and compliance with FDA, IRB, and GCP guidelines. Monitor safety..., and execution of multiple concurrent clinical research studies, including NIH-sponsored, industry-sponsored, and investigator...
databases, and ensure accurate data collection/entry. Manage regulatory binders, IRB submissions, and compliance with FDA, IRB... of multiple concurrent clinical research studies, including NIH-sponsored, industry-sponsored, and investigator-initiated trials...