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Clinical Protocol Development:
- Lead the development and drafting of clinical research protocols in collaboration with study chairs and committees.
- Ensure protocols meet regulatory and departmental standards for accuracy and consistency.
- Oversee protocol amendments and final study closure documentation.
Document Coordination and Quality:
- Prepare and maintain study-related documents including informed consent forms and training materials.
- Review case report forms for consistency with approved protocols.
- Facilitate communication between investigators, coordinators, and external research organizations.
Study Planning and Stakeholder Collaboration:
- Establish development objectives and coordinate weekly study meetings.
- Design experimental study schemas and therapy delivery maps.
- Identify documentation inconsistencies and coordinate necessary amendments to support timely study activation.
Jobgether
Our partner is a collaborative research organization focused on advancing treatments for childhood and adolescent cancer through clinical trials. They are mission-driven and growing, with a small but dedicated team.