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Clinical Trial Oversight:
- Directs protocol implementation, site identification, and communication.
- Monitors clinical trials, overseeing all aspects of trial conduct and safety.
- Interacts with investigators, site study staff, and regulatory agencies.
Program Management:
- Manages program development, working cross-functionally.
- Collaborates with pre-clinical, manufacturing, and other teams.
- Applies knowledge to articulate therapeutic strategies.
Data Analysis and Reporting:
- Supports data analysis and assembly.
- Contributes to clinical study report writing.
- Prepares abstracts, presentations, and manuscripts.
Iovance Biotherapeutics
Iovance is committed to cultivating and offering a diverse and inclusive work environment as an equal-opportunity employer.