Hybrid Clinical Trial Specialist

Regeneron Pharmaceuticals Inc.; New York (NY); Hybrid; USD 94,000 - 153,000; Full time

Job summary

Regeneron Pharmaceuticals Inc. in Armonk, NY is seeking a Clinical Study Specialist to join the Clinical Trial Management team. You will provide technical and administrative support to study teams, helping ensure trials stay on track from site activation through close-out, collaborating with leads, CROs, and study sites.

This role offers cross-functional collaboration and impact across programs. This position features on-site work with hybrid flexibility in a fast-growing, science-driven

Qualifications

• Bachelor's degree with 2+ years of industry-related work experience in a clinical setting.
• Ability to acquire working knowledge in trial management systems and MS applications.
• Basic familiarity with medical terms and clinical drug development.

Responsibilities

• Organizes and delivers analyzable reports and metrics, and coordinates study team meetings, agendas, and minutes
• Collates data for feasibility and site selection assessments, and reviews study documents and reference materials
• Tracks site activation, enrollment, and monitoring visits against plans, escalating issues as needed
• Ensures timely receipt of reports and performs TMF reconciliations with study lead guidance
• Communicates with sites and maintains strong internal and external relationships
• Contributes to close-out activities and oversees third-party vendors as needed
• Participates in SOP revisions and departmental initiatives, recommending process improvements

Skills

Attention to detail

Deadline management

Relationship building

Education

Bachelor's degree

Tools

Project

PowerPoint

Word

Excel

IVRS/IWRS

EDC

TMF

Job description

Regeneron Pharmaceuticals Inc. in Armonk, NY is seeking a Clinical Study Specialist to join the Clinical Trial Management team. You will provide technical and administrative support to study teams, helping ensure trials stay on track from site activation through close-out, collaborating with leads, CROs, and study sites.

This role offers cross-functional collaboration and impact across programs. This position features on-site work with hybrid flexibility in a fast-growing, science-driven