Role OverviewResponsible for coordinating the approval processes and conduct of research protocols, maintaining the integrity and quality of clinical/translational research.
What You Will Do
Prepare and process new IRB research proposals, amendments, continuing review applications, and adverse event reports; accurately prepare and maintain documents required for regulatory authorities and/or the sponsor.
Why It Might Be a Fit
The role requires experience in clinical research, obtaining informed consent, educating patients, and managing clinical research data. The ideal candidate will have strong attention to detail, excellent communication and collaboration skills, and the ability to work effectively with patients, families, investigators, and multidisciplinary teams.
Requirements
- Clinical research experience in a patient-facing research setting
- Experience obtaining informed consent and educating patients
- Familiarity with CITI training and clinical research compliance requirements
- Experience with patient screening, eligibility assessments, and protocol implementation
- Knowledge of regulatory processes, IRB requirements, and clinical research documentation
- Experience collecting, managing, and maintaining accurate clinical research data
- Proficiency with electronic data capture systems, research databases, and related technology platforms
Benefits
- Health insurance
- Disability insurance
- Retirement offerings
- Wellness offerings
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