Oncology Research Specialist - Pediatrics
About The Position
This role assists with clinical, regulatory, business, and other documentation associated with oncology research projects/clinical trials within the department. The specialist participates in study project start-up activities, works with the PI and others to initiate new research projects, and maintains protocol amendments, deviations, and informed consent changes. They ensure all documentation is managed compliantly and maintained in an audit-ready manner, and assists in the maintenance of filing systems, data repositories, and systems. The role also involves monitoring clinical trial compliance by reporting issues and problems appropriately, obtaining required documentation to assess patient eligibility for research studies, and contacting local research staff to confirm scheduling of tests/treatments required by protocol. Additionally, the specialist obtains and completes data for patients enrolled on clinical trials.
Requirements
- High School Diploma or GED required
- Must speak and read/write clearly in English.
- Must be able to be mobile within the entire healthcare system and other locations that participate in clinical trials.
Nice To Haves
- Bachelor's degree preferred, Health/Science preferred.
- Experience in a healthcare setting preferred, especially cancer care and/or clinical research.
- Certification in clinical research (SoCRA, ACRP, RAPS, etc.) preferred.
Responsibilities
- Assists with clinical, regulatory, business, and other documentation associated with oncology research projects/clinical trials within department.
- Participates in the study project start-up activity, works with the PI and others to initiate new research projects.
- Maintains protocol amendments, deviations, and informed consent changes regarding oncology research studies, assures all documentation is managed compliantly and maintained in an audit-ready manner.
- Maintains appropriate documentation for assigned studies.
- Assists in maintenance of filing systems, data repositories and systems.
- Assists in the monitoring of clinical trial compliance by reporting issues and problems appropriately.
- Obtains required documentation and to assess patient eligibility for research studies.
- Contacts local research staff to confirm scheduling of tests/treatments required by protocol.
- Obtains and completes data for patients enrolled on clinical trials.
Benefits
- Comprehensive suite of Total Rewards
- Competitive compensation
- Generous retirement offerings
- Programs that invest in your career development
- Paid Time Off programs
- Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
- Flexible Spending Accounts for eligible health care and dependent care expenses
- Family benefits such as adoption assistance and paid parental leave
- Defined contribution retirement plans with employer match and other financial wellness programs
- Educational Assistance Program
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
