Support the Lead Epi Scientists by providing overall operational support for study conduct
Responsible for the coordination and execution of observational or non-interventional research studies (including Post Authorization studies)
Manages several complex activities and study types
Operational planning and project management of epidemiology research studies
Execution, and close out of primary data collection, chart review, database, and molecular epidemiology studies
Manage vendors including qualification efforts, confidentiality agreements, specifications, and contract reviews
Assist with review and finalization of all vendor documents
Participate in protocol and interim/final report preparation
Coordination of collection, international shipment, processing by internal/external labs and data transfer for biospecimen
based studies
Participate in quality control assessments and ensure integrity of study data for reports and publications
Collaborate extensively and troubleshoot issues
Requirements
Bachelor's degree required in public health (or closely related discipline, such as biostatistics, epidemiology, health administration or biological sciences)
Master's degree (preferred)
Five (5)+ years of work experience within clinical/observational research or equivalent experience; or PhD with 3+ years relevant career experience
Knowledge of epidemiology and/or outcomes research
Strong project management and prioritization skills
Benefits
medical, dental, vision healthcare and other insurance benefits (for employee and family)