Clinical research specialist oncore
The Clinical Research Specialist will manage OnCore, a specialized Clinical Trials Management Software Suite program with an emphasis in Oncology research. The OnCore specialist will primarily be responsible for the following: - Monitoring Quality Assurance (QA) of data within the OnCore system and will perform routine QA checks and analysis via various OnCore reporting tools. - Closely monitor use and data integrity of the OnCore system and overall functionality - Responsible for protocol calendar management (new studies, amendments, updates) - Responsible for building financial console and relevant updates through the life of the trial - Interacts closely with all clinical trial staff and some faculty to assist with training, trouble shooting, and following up on proper use of OnCore system - Seek regular feedback on the functionality of the CTMS with end users and facilitate requests for improvements with the Vendor. - Identifies improvements in workflows, system and makes recommendations to enhance use of CTMS and/or activating functionality - Provides technical assistance and support for incoming queries and issues related to OnCore - Test system software upgrades prior to deployment - Represent the institution on relevant user groups held through the CTMS vendor - May assist with writing training manuals - May write training manuals, FAQs, newsletters or other similar documents for dissemination to end users - May provide regular data entry in the CTMS to include registration of studies and subjects - Assist with the maintenance of clinical research web pages - Assists with roll out of new functionality - Assists with the creating/developing or running of required Cancer Institute reports and/or reports requested by senior administration and various other departments - Assist with mandatory reporting requirements and SOP development, process development or other workflow tools. - Assists OnCore administrator with other appropriate tasks as needed.
- Performs other duties as assigned and may participate in other cores as applicable
ACRP/SoCRA (or equivalent) certification preferred.
Three (3) years minimum experience in area of research specialty.
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- Working Title: Clinical Research Specialist - OnCore
- Department: SOCCI Clinical Research Office
- Business Entity: Academic / Research
- City: Los Angeles
- Job Category: Academic/Research
- Job Specialty: Research Studies/Clinical Trials
- Position Type: Full-time
- Shift Length: 8 hour shift
- Shift Type: Day