Clinical Data Manager

Clinical Data Manager

Full-Time 40000 - 50000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead clinical research tasks and analyse complex medical data to enhance innovative treatments.
  • Company: Join ICON, a global leader in healthcare intelligence and clinical research.
  • Benefits: Enjoy competitive salary, health coverage, and career development opportunities.
  • Other info: Collaborative environment with a focus on inclusion and professional growth.
  • Why this job: Make a real impact in healthcare while working with cutting-edge data management technologies.
  • Qualifications: Bachelor's degree in Life Sciences or Healthcare and experience in clinical data management.

The predicted salary is between 40000 - 50000 £ per year.

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.

As a Senior CDC at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will lead on clinical research tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include:

  • Create and maintain detailed data management plans and documentation, ensuring compliance with industry standards and regulatory requirements.
  • Participate in the identification and resolution of data discrepancies and issues, working to streamline data flow and enhance data quality throughout the study lifecycle.
  • Collaborate closely with cross-functional teams, including clinical operations and biostatistics, to develop and execute data management strategies tailored to specific studies.
  • Perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation, dispatching of queries to investigator sites for resolution, etc.).
  • Mentor junior data coordinators, providing expert guidance on data reconciliation, coding, and cleaning procedures.
Your Profile:

You will have a strong foundation in clinical research, with the experience to work independently and guide others.

Required qualifications and experience:
  • Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
  • Proven experience in clinical data management within the pharmaceutical or biotechnology industry.
  • Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).
  • Strong attention to detail and the ability to work effectively in a fast-paced environment.
  • Excellent communication skills and the ability to collaborate with cross-functional teams.
  • Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.
  • Willingness to travel as required (approximately 5%).

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 programmes including medical, dental, and vision coverage where applicable.
  • Retirement and pension plans.
  • Life assurance and disability coverage.
  • Employee assistance programmes and wellbeing resources.
  • Learning and development opportunities through structured training and career pathways.

Benefits may vary depending on role and location.

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.

Clinical Data Manager employer: IRE

ICON is an exceptional employer for Clinical Data Managers, offering a dynamic work environment that prioritises integrity, collaboration, and inclusion. With a strong focus on employee growth through structured training and career pathways, ICON provides competitive salaries, comprehensive health benefits, and a commitment to wellbeing, making it an ideal place for professionals looking to make a meaningful impact in the healthcare sector.

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Contact Details:

IRE Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Clinical Data Manager

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We think you need these skills to ace Clinical Data Manager

Clinical Data Management
Data Management Plans
Regulatory Compliance
Data Discrepancy Resolution
Data Quality Enhancement
Cross-Functional Collaboration
Data Management Software (e.g., Medidata, Oracle RDC)

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at IRE!

Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show IRE that you're not just a fit for the job but also a safety-conscious candidate!

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How to prepare for a job interview at IRE

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at IRE that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

Showcase Relevant Experience

If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

Know Their Products

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