Associate Project Manager (Clinical Biometrics)

Location: United States; remote role

Company

hirify.global is a global full-service CRO delivering clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

What you will do

• Support project plans, timelines, milestones, deliverables, resource requirements, and coordination across Biostatistics, Statistical Programming, and Data Management.
• Track study progress against contracted scope, timelines, milestones, budgets, and hours.
• Support database lock, analysis, reporting, and other critical biometrics milestones across multiple studies or workstreams.
• Prepare agendas, status updates, meeting minutes, action trackers, and facilitate routine project meetings as experience develops.
• Maintain risk, issue, decision, and action logs; support mitigation and recovery plans and escalate potential delays or scope, resource, and quality issues.
• Support quality, compliance, inspection readiness, audit readiness, change-order preparation, forecasts, and project financial updates.

Requirements

• Bachelor’s degree or higher in life sciences.
• 0–2 years of relevant experience in the pharmaceutical or CRO industry, with a basic understanding of clinical drug development and clinical trials.
• Familiarity with project management concepts including scope, timelines, budgets, risks, dependencies, and change control.
• Knowledge of FDA regulations, drug development processes, project management processes, and ICH/GCP guidelines.
• Strong written and verbal communication, organization, time management, attention to detail, follow-through, teamwork, and customer focus.
• Proficiency with Microsoft Word, Excel, PowerPoint, Outlook, and MS Project.

Nice to have

• MBA or PMP certification.
• Experience in project coordination, clinical operations, Data Management, Biostatistics, Statistical Programming, or another biometrics function.

Culture & Benefits

• Work within a global CRO serving pharmaceutical, biotechnology, medical device, and consumer health organizations.
• Access to continuous training focused on internal and client processes, competence, and professional expertise.
• Collaborative and diverse environment guided by inclusivity and equal opportunity.
• Opportunity to contribute to the development and commercialization of innovative drugs and medical devices.