Written And Verbal Communication Jobs in Florham Park, NJ

OverviewThe Associate Director GCP/GVP Quality Assurance provides senior-level quality oversight for Shionogis clinical development and pharmacovigilance activities ensuring compliance with ICH FDA EMA PMDA MHRA and other global regulatory requirements. Serving as the QA representative to assigned s...

OverviewThe Senior Director Field Medical Affairs (FMA) in COVID-19/Virology will be responsible for providing leadership oversight and overall direction to a group of US Medical Science Liaisons (MSLs). Will oversee and manage the MSL Team in cultivating Key Opinion Leaders (KOLs) and emerging thou...

OverviewThe Director Field Medical Affairs (FMA) in COVID-19/Virology is responsible for leading and managing a regional team of Medical Science Liaisons (MSLs) driving scientific engagement and supporting the tactical execution of medical affairs strategies for COVID-19/Virology. This role ensures...

OverviewThe PV Quality Assurance Specialist will provide operational support to the Pharmacovigilance / Patient Safety (PSPV) team in maintaining a compliant global PV system. The role is responsible for reviewing quality system documentation supporting deviation and CAPA management and contributing...

OverviewThe Product Safety & Pharmacovigilance (PSPV) Manager is responsible for overseeing and managing the PSPV team ensuring efficient case processing safety information management in clinical trials compliance with corrective and preventive actions (CAPA) audit and inspection correspondence team...

OverviewThe Clinical Research Scientist will review and interpret clinical data for query resolution by contacting clinical study site personnel including the principal investigator.Responsible for authoring editing and reviewing complex clinical study documents in collaboration with the Global Medi...

OverviewThe Senior Promotional Review Associate (Contractor) will provide operational and coordination support to the U.S. Review Committee (USRC) process for assigned products. This role will assist with preparing promotional materials for review facilitating meetings maintaining documentation in V...

OverviewThis role will support the Regulatory Operations team with the preparation of submission related documentation for electronic submission. The scope of this role includes assisting in document formatting remediation and quality control (QC) of documentation for submissions to Health Authoriti...

This role supports US Commercial Learning & Development to design and implement digital learning solutions for the sales force. Responsibilities include leading and implementing learning technology projects from start to finish overseeing validation and documentation and delivering training on platf...