Project Manager - Clinical Studies

As a Project Manager in our Compliance, Quality, and Regulatory team, you will drive transformative clinical IT programs within the pharmaceutical and clinical domains. You will collaborate with major pharmaceutical clients to deliver patient-focused, compliant, and efficient digital solutions that modernize clinical trials and planning processes. In this role, you will lead cross-functional teams, manage project timelines, and ensure delivery meets regulatory requirements, industry standards, and business goals. Your ability to bridge business analysis, project management, and IT expertise will be crucial in driving success.

Your Profile
Required Experience:
• Degree in business, IT, engineering, or a related field.
• Extensive experience in project management within clinical IT and pharmaceutical domains.
• Proficiency with Agile methodologies, Scrum Master frameworks, and project management tools.
• Strong background in business analysis, requirements gathering, and stakeholder management.
• Experience leading large-scale transformation programs.
• Fluency in spoken and written English.

Meritorious:
• Experience in life sciences or digital health solutions.
• Familiarity with clinical trial processes, consent workflows, and regulatory compliance (e.g., GDPR, GxP).
• Knowledge of clinical data management tools and processes.

You as a Person
We seek a proactive, broad-skilled project manager who thrives in a fast-paced environment, navigates complexity, and drives results. You should be adaptable, solutions-focused, and capable of balancing technical and business perspectives. Your leadership, communication skills, and ability to motivate teams will set you apart. At Capgemini Engineering, we value excellence, care, responsibility, dynamism, and innovation. We offer diverse projects, career development opportunities, and a collaborative environment where your contributions make a difference in advancing healthcare and technology.

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