Clinical Project Manager — Pharma Data & Ops Leader

Cytel; Little Rock (AR); On-site; USD 85,000 - 120,000; Full time

Job summary

Cytel is seeking a Project Manager to lead cross-functional teams in a sponsor-dedicated clinical development setting. You will coordinate data standards, statistics programming, and operational transitions across programs, while maintaining documentation and ensuring inspection readiness.

You’ll partner with Data Management, Biostatistics, and Clinical Operations to deliver on timelines and sponsor expectations.

Qualifications

• Bachelor's degree in Life Sciences, Statistics, Computer Science, or related field.
• 5+ years in clinical research, CRO, pharmaceutical, or biotechnology environments.
• 2+ years of project management or study management experience.
• Working knowledge of the clinical development lifecycle.

Responsibilities

• Coordinate and track clinical data standards and statistical programming activities across clinical programs
• Support operational transition activities including organizing workshops for knowledge transfer, identifying/maintaining procedural documents, training planning and creating checklist and documentation inventory
• Support inspection readiness and ensure appropriate project documentation is maintained
• Develop and maintain task lists, process flow, project plans, timelines, resource forecasts, risk logs, and communication plans
• Help to build internal portal to support future activities
• Support to update SOPs as needed
• Facilitate cross-functional project meetings and communicate project status to internal teams and sponsor stakeholders
• Utilizing your strong communication skills to present and explain the methodology and consequences of decisions

Skills

Project management

Cross-functional coordination

Stakeholder management

Communication

Documentation

Education

Bachelor's degree in Life Sciences/Statistics/CS

Job description

Cytel is seeking a Project Manager to lead cross-functional teams in a sponsor-dedicated clinical development setting. You will coordinate data standards, statistics programming, and operational transitions across programs, while maintaining documentation and ensuring inspection readiness.

You’ll partner with Data Management, Biostatistics, and Clinical Operations to deliver on timelines and sponsor expectations.