Safety & Pharmacovigilance Opportunities at INC Research

Safety & Pharmacovigilance Opportunities at INC Research

Explore Careers at INC Research

Summary: Performs all aspects of the collection, processing, and reporting of adverse events/endpoints adhering to all data protection guidelines, Health Insurance Portability and Accountability Act (HIPAA), Good Clinical Practices (GCPs), regulatory guidelines, and study procedures. May lead or oversee one or several projects of various levels of complexity. Manages...

17003011 Requisition #

Learn More

Summary: Performs all aspects of the collection, processing, and reporting of adverse events/endpoints adhering to all data protection guidelines, Health Insurance Portability and Accountability Act (HIPAA), Good Clinical Practices (GCPs), regulatory guidelines, and study procedures. May lead or oversee one or several projects of various levels of complexity. Manages...

17003010 Requisition #

Learn More

Summary: Performs all aspects of the collection, processing, and reporting of adverse events/endpoints adhering to all data protection guidelines, Health Insurance Portability and Accountability Act (HIPAA), Good Clinical Practices (GCPs), regulatory guidelines, and study procedures. May lead or oversee one or several projects of various levels of complexity. Manages...

17003009 Requisition #

Learn More

Summary: Provides medical expertise to the safety and pharmacovigilance department, in both clinical trials and post-marketing. Contributes to the analysis, review and approval of Individual Case Safety Reports (ICSR) and Periodic Reports for marketed and investigational products. Maintain active pharmacovigilance oversight for products including accurate signal...

17003006 Requisition #

Learn More

Summary: Performs all aspects of the collection, processing, and reporting of adverse events/endpoints adhering to all data protection guidelines, Health Insurance Portability and Accountability Act (HIPAA), Good Clinical Practices (GCPs), regulatory guidelines and study procedures. May lead one or several projects of moderate to high complexity.Essential Functions:...

17002843 Requisition #

Learn More

Do you want to be a part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for...

17001699 Requisition #

Learn More

Summary: Performs all aspects of the collection, processing, and reporting of adverse events/endpoints adhering to all data protection guidelines, Health Insurance Portability and Accountability Act (HIPAA), Good Clinical Practices (GCPs), regulatory guidelines and study procedures. May lead one or several projects of moderate to high complexity.Essential Functions:...

17002740 Requisition #

Learn More

Summary: Provides administrative support to the Safety and Pharmacovigilance department staff while adhering to all data protection guidelines, Health Insurance Portability and Accountability Act (HIPAA), Good Clinical Practices (GCPs), regulatory guidelines, and study procedures.Essential Functions: Records all adverse event/endpoint source documentation and tracks them...

17002844 Requisition #

Learn More

Summary: Provides administrative support to the Safety and Pharmacovigilance department staff while adhering to all data protection guidelines, Health Insurance Portability and Accountability Act (HIPAA), Good Clinical Practices (GCPs), regulatory guidelines, and study procedures.Essential Functions: Records all adverse event/endpoint source documentation and tracks...

17001644 Requisition #

Learn More

Summary: Provides administrative support to the Safety and Pharmacovigilance department staff while adhering to all data protection guidelines, Health Insurance Portability and Accountability Act (HIPAA), Good Clinical Practices (GCPs), regulatory guidelines, and study procedures.Essential Functions: Records all adverse event/endpoint source documentation and tracks...

17002448 Requisition #

Learn More
Back to Top