Senior Clinical Research Coordinator: Study Operations

Medical University of South Carolina; Charleston (SC); Presencial; USD 62 405 280 - 106 212 960; Tempo integral

Resumo da oferta

The Medical University of South Carolina is seeking a Senior Clinical Research Coordinator to oversee day-to-day coordination of complex clinical studies. You will ensure protocol adherence, regulatory compliance, and high-quality data management across multiple sites.

Responsibilities include participant screening and consent, coordinating visits, SAEs reporting, and sponsor communications, with potential after-hours work and travel as needed.

Qualificações

• Bachelor's degree and three years of relevant program experience.
• Knowledge of GCP and regulatory requirements.
• Ability to coordinate complex studies and sponsor interactions.

Responsabilidades

• Coordinate and manage assigned clinical research studies per protocol and GCP.
• Screen, enroll, and consent participants; monitor safety and report SAEs.
• Maintain accurate source data, CRFs, and study documentation for audits.

Conhecimentos

GCP

Clinical coordination

Informed consent

Data management

Study documentation

Formação académica

Bachelor's degree

Ferramentas

Epic

Excel

EDC

Descrição da oferta de emprego

The Medical University of South Carolina is seeking a Senior Clinical Research Coordinator to oversee day-to-day coordination of complex clinical studies. You will ensure protocol adherence, regulatory compliance, and high-quality data management across multiple sites.

Responsibilities include participant screening and consent, coordinating visits, SAEs reporting, and sponsor communications, with potential after-hours work and travel as needed.