What are the responsibilities and job description for the Associate Director, Clinical Systems position at Pacira Pharmaceuticals?
About Pacira BioSciences, Inc.
Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for healthcare practitioners and their patients. Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results.
Why work with us? Rarely do you have an opportunity to do work that really matters. What drives us is our mission. What makes us successful are our people. At Pacira, you are part of an inclusive culture that fosters collaboration, growth, and innovative thinking - a place where you can make an impact and help change the standard of care in non-opioid pain management. Be part of our movement, let's pursue excellence together.
Job Summary
The Associate Director, Clinical Systems will support and develop capabilities for clinical data acquisition and standardization, increase efficiency of database builds, data visualization, and enable compliance to CDISC standards (e.g. CDASH, SDTM) while implementing industry best practices.
Key Responsibilities
- Clinical Systems Support: Expert in clinical systems and platforms (e.g. Medidata, Veeva CDMS, Veeva CTMS, CliqSense, JReview) configurations, capabilities, and system behaviors. Lead and deliver new capabilities, innovative technical solutions and/or clinical system integrations that enable future proof study execution.
- Technical support for system integration, patient facing technologies and data reporting tools (e.g., IRT, ePRO). Ensure continuous improvement of processes, tools and outputs to be used to facilitate advancement of study portfolio.
- Liaise with systems vendors to develop and maintain system environments to support the organization. Lead efforts to identify future system capability and enhancement opportunities.
Study Support
- Technical study lead to work with study team counterparts on study deliverables from external partners (e.g. Functional Service Providers, CROs, technology providers) performing data collection and data visualization services on behalf of Pacira.
- Oversee the build, maintenance, and deployment of study databases to collect clinical trial data, including configuring custom integrations if applicable.
- Oversee the build, maintenance, and deployment of data visualizations to display clinical trial data, including configuring custom integrations if applicable.
- Manage work assignments to ensure timely delivery of study databases, data review reporting, external data management, and other study related technical components.
Standards
- Responsible for ensuring the activities required to build out standard objects (e.g., eCRF forms, edit checks, eCRF entry guidelines, standard data review reports) that are compliant with CDISC (SDTM) are implemented.
- Collaborate with cross functional core roles (Data Managers, Medical Monitors, Statisticians, Programmers, etc.) to implement new or modified global library objects.
- Develop and monitor key standard clinical systems performance metrics.
Education and Experience
- BS/BA degree in a relevant scientific discipline required.
- 8 years of experience in clinical systems execution and support, including EDC, data visualization, and data standardization preferred.
- Minimum 5 years of experience leading process management and innovation.
Salary
$123,456 per year
Benefits
MEDICAL INSURANCE PRESCRIPTION DENTAL VISION COVERAGE FLEXIBLE SPENDING ACCOUNT & HEALTH SAVINGS ACCOUNT WITH COMPANY MATCH EMPLOYEE ASSISTANCE PROGRAM MENTAL HEALTH RESOURCES DISABILITY COVERAGE LIFE INSURANCE CRITICAL ILLNESS AND ACCIDENT INSURANCE LEGAL AND IDENTITY THEFT PROTECTION PET INSURANCE FERTILITY AND MATERNITY ASSISTANCE 401(K) WITH COMPANY MATCH FLEXIBLE TIME OFF (FTO) AND 11 PAID HOLIDAYS PAID PARENTAL LEAVE
Salary : $123,456
