Oncology Research Specialist - Phase 1
Overview
Lead oncology research initiatives supporting clinical trials at Atrium Health. Drive study start-up processes and maintain compliance documentation. Collaborate with principal investigators to ensure accurate patient eligibility assessments and protocol adherence.
What You'll Do10
- 1Assist with clinical regulatory business documentation for oncology research projects
- 2Participate in study project initiation and ongoing monitoring activities
- 3Manage protocol amendments and deviations ensuring audit readiness
- 4Maintain filing systems and data repositories for clinical trials
- 5Monitor trial compliance through issue reporting and problem assessment
- 6Obtain required patient documentation and verify eligibility criteria
- 7Coordinate test and treatment scheduling with local research staff
- 8Complete clinical trial data collection for enrolled patients
- 9Perform physical tasks including occasional lifting of 35-pound items
- 10Provide clear communication in English while maintaining professional documentation standards
Requirements9
- 1High school diploma or GED required
- 2Bachelor's degree preferred in health science or related field
- 3Certification in clinical research such as SoCRA or ACRP
- 43-5 years of experience in healthcare settings
- 5Proficiency with AWS and React frameworks
- 6Understanding of Spark and Airflow for data engineering tasks
- 7Ability to travel throughout healthcare system network
- 8Strong written and verbal communication skills in English
- 9Full mobility required for workplace demands
Salary Insight
$52 - $77k per year
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