Hiring.Camp

Clinical Research Data Coordinator

Nebraska Cancer Specialists

·

Today

Location
Omaha, NE
Department
Healthcare
Education
Associate
Source
Paylocity

Description

Description

Do you have a passion for Oncology/Hematology?


Nebraska Cancer Specialists (NCS) is committed to providing state of the art care to our patients with oncologic and hematologic disorders in a compassionate and caring manner, and to advance cancer treatment through research and education. We continuously strive to be known as the most knowledgeable, progressive, trusted and compassionate cancer practice in the region.  


NCS  is currently seeking a Clinical Research Data Coordinator.  This position will be responsible for the collection, coordination and quality control of clinical trial data. 


What’s in It for You? We know you work hard, and we believe in rewarding that! Here’s what you’ll love about NCS:


Monday-Friday schedule – No nights, weekends, or holidays!

Generous PTO – Plus holidays and your birthday off!

Affordable health, dental, and vision insurance

Employer-paid benefits – Short & long-term disability, life insurance, and EAP services

401(k), HSA, and FSA options – Plan for your future with confidence!

CEU/Conference allowance – Keep growing in your field!

Extra perks – Because you deserve it


Job Duties:

  • Extrapolate data, complete case report forms and ensure data submission.
  • Train on various trial systems including, but not limited to Clinical Trials Management System, local clinical trials database and other resources available to access research forms and keep current all applicable patient reporting and tracking functions.
  • Actively prepare for/participate in monitoring and auditing activities.
  • Create process ensuring all queries are resolved.
  • Collect survival data and report to sponsor.
  • Responsible for updating screening enrollment logs for study protocols.
  • Schedule study monitor visits.  Set up profiles for research monitors within the EMR system.
  • Contact physician or referring physician offices for data follow up on research patients
  • Initiate Serious Adverse Event Reporting and follow up.
  • Work in compliance with all applicable research entities and federal, state, and local regulatory bodies.

Requirements

Associate degree or relevant experience in a clinical or scientific related discipline desired.


NCS is an equal opportunity employer and participates in E-verify. All offers are contingent upon successful completion of references, criminal background checks, abuse registry checks, and a post-offer drug and alcohol screen. 

Skills

EMRClinical TrialsCompliance

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