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Weekend Oncore Jobs (NOW HIRING)

... weekends. Moffitt offers training and orientation. Position Summary: The primary focus of this ... Preferred knowledge of EMR system (Powerchart) and clinical trial management systems (OnCore)

Experience with Stanford systems (REDCap, eProtocol, OnCore, SeRA). * Knowledge of IRB processes ... Occasional evening or weekend hours may be required for study visits or participant needs. * Must ...

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Weekend Oncore information

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$245K

$376.7K

$400K

How much do weekend oncore jobs pay per year?

As of Aug 22, 2026, the average yearly pay for weekend oncore in the United States is $376,749.00, according to ZipRecruiter salary data. Most workers in this role earn between $371,000.00 and $400,000.00 per year, depending on experience, location, and employer.

What cities are hiring for Weekend Oncore jobs?

Cities with the most Weekend Oncore job openings:

What are the most commonly searched types of Oncore jobs?

The most popular types of Oncore jobs are:

What states have the most Weekend Oncore jobs?

States with the most job openings for Weekend Oncore jobs include:

Infographic showing various Weekend Oncore job openings in the United States as of July 2026, with employment types broken down into 15% Locum Tenens, 49% As Needed, 2% Full Time, 15% Temporary, 18% Nights, and 1% Summer. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $376,749 per year, or $181.1 per hour.

$24 - $32/hr

Full-time

Re-posted 11 days ago


Job description

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena.

Responsibilities:

  • Assure all study requirements are met and documented and meet both internal and external regulations in accordance with protocol guidelines. 
  • Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs. 
  • Design systems for coordinating, compiling and submission of data; design workflow processes and participate in quality assurance measures; coordinate site visits. 
  • Manage all patient and/or protocol data as assigned and respond to queries in a timely fashion. 
  • Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required.


 

         Bachelor's degree required or equivalent combination of education and experience.

         Medical and/or science experience/education preferred.

         Clinical research certification preferred.

Equal Opportunity Employer of Minorities/Females/Disabled/Veterans


Additional Information
  • Schedule: Full-time
  • Requisition ID: 26002859
  • Daily Work Times: 8am-4:30pm
  • Hours Per Pay Period: 80
  • On Call: No
  • Weekends: No