Clinical Research Nurse Pediatric Hematology Oncology
Overview
The position owns monitoring and assessment of study-related side effects for Neuro-oncology trials while supporting the Principal Investigator. It coordinates clinical data reporting and sample processing to ensure accurate submission to sponsors and regulators.
What You'll Do11
- 1Assess and report clinical data accurately to sponsor and regulatory authorities
- 2Coordinate collection and processing of pharmacokinetic samples
- 3Develop and improve study procedures to resolve operational challenges
- 4Design recruitment strategies and enroll subjects using IRB approved methods
- 5Manage specimen handling shipping and documentation
- 6Communicate lab findings with laboratory and sponsor teams
- 7Document protocol deviations and maintain GCP compliance
- 8Prepare and submit IRB documents such as consent forms and protocols
- 9Schedule monitor visits and provide training to study personnel
- 10Maintain inventory of study materials and ensure regulatory documentation
- 11Compose and respond to audit reports from sponsors and FDA
Requirements7
- 1Bachelor's degree in nursing with one year clinical experience
- 2Licensed Practical Nurse upon hire
- 3Society of Clinical Research Associates certification preferred
- 45+ years of clinical nursing experience
- 5Ability to handle multiple priorities under deadline pressure
- 6Strong interpersonal communication skills
- 7Experience in regulated environments with financial analysis capabilities
Salary Insight
$75 - $85k per year
Location
Required Skills
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