Clinical Project Manager: Autonomous Cross-Functional Leader

Cytel

Honolulu (HI)

On-site

USD 90,000 - 120,000

Full time

11 days ago
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Job summary

Cytel is seeking a Project Manager to lead cross-functional teams in pharmaceutical and clinical development environments. You will drive operational transformation, process optimization, and documentation maintenance for clinical activities.

Responsibilities include coordinating data standards, vendor management, and keeping stakeholders informed. A strong background in clinical programming and lifecycle understanding is required.

Qualifications

  • Bachelor's degree required in Life Sciences, Statistics, Computer Science, or related field.
  • 5+ years of experience in clinical research, CRO, pharmaceutical, or biotech environments.
  • 2+ years of project management or study management experience.
  • Experience with clinical development lifecycle and cross-functional coordination.

Responsibilities

  • Coordinate and track clinical data standards and statistical programming activities across clinical programs.
  • Support operational transition activities, workshops, knowledge transfer, and documentation inventories.
  • Ensure inspection readiness and maintain project documentation.
  • Develop and maintain task lists, processes, timelines, and risk logs.
  • Facilitate cross-functional project meetings and communicate status to sponsors.

Skills

Project management
Cross-functional collaboration
Communication
Organizational skills
Stakeholder management
Problem-solving

Education

Bachelor's degree in Life Sciences, Statistics, Computer Science, or related field

Tools

SDTM
ADaM
TFLs
ISS/ISE

Job description

Cytel is seeking a Project Manager to lead cross-functional teams in pharmaceutical and clinical development environments. You will drive operational transformation, process optimization, and documentation maintenance for clinical activities.

Responsibilities include coordinating data standards, vendor management, and keeping stakeholders informed. A strong background in clinical programming and lifecycle understanding is required.

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