Description Participates in components of the clinical trial development, implementation, maintenance, and completion process as directed. Responsibilities may include but are not limited to: assisting with protocol/clinical research development and maintenance including gathering regulatory documents, drafting the informed consent, developing clinical trial budgets, identifying/coordinating study logistics/approvals and protocol modifications. Must be able to work in a complex environment and …
Completá tu perfil y te avisamos cuando se publiquen concursos y oportunidades laborales en las cuales puedas aplicar o se ajusten a ti.
Para que te mantengamos informado de empleos como este — Research Protocol Associate - Cancer Center
Deja de buscar. Tu próximo trabajo ya está en tu bolsillo. Oportunidades que se adaptan a ti, no al revés.