Clinical research specialist oncore

Cedars-sinai - Los Angeles
new offer (27/05/2020)

job description

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

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Educational Requirements:

 BA/BS degree.


License/Certification Requirements:

 ACRP/SoCRA (or equivalent) certification preferred.

Experience:

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

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Clinical research specialist oncore

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