Clinical Project Manager: Lead Timelines, Budgets & Clients

Cytel; Polska; Hybrid; PLN 90,000 - 130,000; Full time

Job summary

Cytel is seeking a Project Manager to lead and manage independent clinical trial projects of moderate complexity, overseeing timelines, budgets, and quality to meet contract specifications. You will coordinate cross-functional teams and communicate with sponsors to ensure satisfaction and project success.

The role requires a bachelor's degree and 3–5 years of PM experience in clinical trials, with strong leadership, communication, and financial management skills.

Qualifications

• Bachelor's degree required.
• 2+ years relevant work experience in clinical trials (Biostatistics, Statistical Programming, or Clinical Data Management).
• 3-5 years of Project Management experience or equivalent.
• Experience managing business operations for clinical trials.

Responsibilities

• In a matrix fashion, lead and manage the project team, in planning and executing the project to meet contractual quality, timeline, and budget expectations and specifications.
• Actively manage client communication, interaction, and satisfaction.
• Actively and proactively manage project timelines, scope and budget, including changes during the life of a project.
• Ensure all relevant project documentation is up to date and follows SOP and other relevant regulations.
• Actively manage project financial performance, to achieve profitability target, and report status and outlook (including revenue, invoicing and forecasting).
• Communicate status of timelines, scope and budget to the sponsor and to Cytel management.
• Act as primary point of contact for assigned customers for general project aspects, especially relating to scope, timeline, budget and quality.

Skills

Communication

Leadership

MS Office

Financial management

Team building

Problem solving

Education

Bachelor's degree

Job description

Cytel is seeking a Project Manager to lead and manage independent clinical trial projects of moderate complexity, overseeing timelines, budgets, and quality to meet contract specifications. You will coordinate cross-functional teams and communicate with sponsors to ensure satisfaction and project success.

The role requires a bachelor's degree and 3–5 years of PM experience in clinical trials, with strong leadership, communication, and financial management skills.