Clinical Study Specialist (Clinical Research)

Location: Armonk, NY or Warren, NJ; primarily onsite with hybrid flexibility

Salary: $93,900–$153,300 annually

Company

hirify.global is a biotechnology company that develops and commercializes medicines for serious diseases.

What you will do

• Provide technical and administrative support to clinical study teams across a program.
• Prepare reports and metrics and coordinate study team meetings, agendas, and minutes.
• Support feasibility assessments, site selection, study document review, and reference material management.
• Track site activation, enrollment, monitoring visits, investigator status, and registry postings, escalating delays when needed.
• Coordinate scheduled reports, TMF reconciliations, site communications, close-out activities, and third-party vendor oversight.
• Contribute to SOP revisions, process improvements, and proactive issue resolution.

Requirements

• Bachelor’s degree and 2+ years of industry-related experience in a clinical setting.
• Working knowledge of trial management systems and Microsoft applications, including Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC, and TMF.
• Basic familiarity with medical terminology and clinical drug development.
• Awareness of ICH/GCP guidelines.
• Proactive, self-disciplined approach with strong deadline and priority management.

Culture & Benefits

• Science-driven environment focused on developing life-changing medicines.
• Inclusive workplace and equal opportunity employment.
• Comprehensive rewards package may include bonuses, equity, retirement benefits, healthcare, insurance, paid time off, and family support benefits.
• Many roles are performed onsite to support collaboration.