Clinical Study Coordinator – Internal Medicine Trials

Regulatory Jobs; Armonk (NY); Híbrido; USD 94.000 - 153.000; Jornada completa

Descripción de la vacante

Regeneron is seeking a Clinical Study Specialist to join our Clinical Trial Management team in Armonk, NY or Warren, NJ. The role provides technical and administrative support to trials from site activation through close-out, collaborating with study leads, CROs, and sites.

The position offers on-site work with hybrid flexibility, and a comprehensive rewards package. A Bachelor’s degree and 2+ years of clinical experience are required, with familiarity with ICH/GCP and trial management tools.

Formación

• Bachelor's degree with 2+ years of industry-related work experience in a clinical setting.
• Experience with trial management systems and MS Office applications.
• Familiarity with medical terms and clinical drug development.

Responsabilidades

• Organizes and delivers analyzable reports and metrics, and coordinates study team meetings, agendas, and minutes.
• Tracks site activation, enrollment, and monitoring visits against projected plans, escalating issues.
• Ensures timely receipt of scheduled reports and performs TMF reconciliations with study lead guidance.
• Communicates with sites and maintains site contact information and relationships.
• Contributes to close-out activities and oversight of third-party vendors as needed.

Conocimientos

Attention to detail

Deadline management

Communication

Educación

Bachelor's degree

Herramientas

PowerPoint

Word

Excel

EDC

TMF

Descripción del empleo

Regeneron is seeking a Clinical Study Specialist to join our Clinical Trial Management team in Armonk, NY or Warren, NJ. The role provides technical and administrative support to trials from site activation through close-out, collaborating with study leads, CROs, and sites.

The position offers on-site work with hybrid flexibility, and a comprehensive rewards package. A Bachelor’s degree and 2+ years of clinical experience are required, with familiarity with ICH/GCP and trial management tools.