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ICON plc

Clinical Data Manager II

Paris
Posted 1 day ago
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Clinical Data Manager, Sponsor Dedicated

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients, and suppliers.

Senior CDSL (Sponsor Dedicated) UK or France

What You Will Do:

You will oversee clinical data science workstreams, ensuring deliverables meet quality and timeline expectations.

Key Responsibilities Include:

  • Leading the development and implementation of clinical data management strategies to optimize data collection, analysis, and reporting.
  • Collaborating with cross-functional teams to ensure the accurate integration of data science techniques into clinical trial designs.
  • Overseeing the analysis of clinical data to provide actionable insights that inform study decisions and outcomes.
  • Providing strategic guidance on data governance, quality control, and compliance with regulatory requirements.
  • Establishing partnerships with key stakeholders to leverage the latest advancements in data science and technology in clinical research.

Required Qualifications and Experience:

  • Bachelor's degree in Life Sciences, Computer Science, or a related field.
  • 8 to 10 years of clinical data management experience, including Early Development and Phase I studies.
  • Experience leading at least three study start-ups and three database locks.
  • Strong knowledge of clinical data management, data review, and data quality processes.
  • Experience participating in User Acceptance Testing and reviewing data reports.
  • Comfortable managing frequent real-time data extractions and supporting rapid study decisions.
  • Experience leading post-production changes and change control activities.
  • Experience overseeing Clinical Data Coordinators and delegated activities.
  • Experience managing external data vendors and third-party data deliverables.
  • Exposure to dose escalation studies and meetings preferred.
  • Strong leadership skills with experience working across cross-functional teams.
  • Proficient in data analysis tools, statistical software, and data visualization.
  • Excellent communication, stakeholder management, and problem-solving skills.
  • Proactive approach with the confidence to research, resolve issues, and drive outcomes.
  • CRO oversight experience preferred but not required.
  • Willingness to travel up to 15 percent as required.

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Employment with ICON

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:

  • Competitive base salary and performance-related incentives
  • Health and wellbeing programs including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

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Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live.

If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

Didn’t find the role you were looking for? Even if the perfect role isn’t available right now, we’re always excited to connect with talented individuals. Register to our Talent Community to receive updates on roles that align with your career goals.

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Skills

Clinical Data Management
Data Science
Data Governance
User Acceptance Testing
Stakeholder Management
Data Visualization
Statistical Software
Change Control
Vendor Management
Clinical Trial Design
Regulatory Compliance
Quality Control

Location

Paris, Ile-de-France, France

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