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Senior Clinical Data Management Analyst

TN United Kingdom

Witney

On-site

GBP 40,000 - 70,000

Full time

14 days ago

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Job summary

Join a vibrant and inclusive team as a Senior Clinical Data Management Analyst in Witney, where you will lead data management activities for clinical trials and R&D projects. This role offers a unique opportunity to develop and maintain processes that enhance the quality of healthcare solutions. Collaborate with diverse teams, implement best practices, and contribute to innovative projects that improve lives globally. With a competitive salary and comprehensive benefits, this position is ideal for detail-oriented professionals looking to make a significant impact in the healthcare sector.

Benefits

Pension
Healthcare
Share Schemes
Flexible Benefits
Wellness Programs
Onsite Activities

Qualifications

  • Experience in a regulated clinical data management environment is advantageous.
  • Ability to manage multiple projects and collaborate effectively.

Responsibilities

  • Lead data management activities supporting Clinical Affairs and R&D.
  • Develop and maintain data management processes and best practices.

Skills

Data Management
Clinical Trials
Communication Skills
Teamwork
Detail-oriented

Education

BSc in a Scientific Discipline

Job description

Social network you want to login/join with:

Senior Clinical Data Management Analyst, Witney

Client:

Abbott

Location:

Witney, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

Job Reference:

8cba52b2642d

Job Views:

10

Posted:

26.04.2025

Expiry Date:

10.06.2025

Job Description:

The Opportunity

In this role, you will join a vibrant, friendly, and inclusive team of Data Managers, EDC programmers, and Statistical Programmers, working across various clinical trials and R&D projects.

Key activities include:

  • Leading and directing data management activities supporting Clinical Affairs and R&D.
  • Developing and maintaining data management processes, procedures, and best practices.
  • Supporting clinical studies, including CRF design/review, database build, validation, and data management documentation.
  • Participating in clinical study teams and coordinating with other departments to establish priorities and schedules.

Essential Skills and Experience

You should hold a BSc or higher in a scientific or technical discipline. Experience in a regulated clinical data management environment is advantageous.

You will be expected to manage multiple projects, collaborate with colleagues from diverse backgrounds, and implement data management processes. You should be adaptable, detail-oriented, possess excellent communication skills, and have strong teamwork abilities.

About Abbott

Abbott is dedicated to health innovation. For over 135 years, we have helped people reach their potential through better health. With a global presence in over 160 countries, we develop solutions across diagnostics, devices, nutrition, and more, to improve lives worldwide.

Our Diabetes Care team in Witney develops glucose monitoring systems, including the innovative FreeStyle Libre series. We are committed to improving quality of life through advanced healthcare technologies.

Abbott offers a competitive salary, comprehensive benefits, including pension, healthcare, share schemes, and flexible benefits. We support our employees' well-being through various initiatives, such as onsite activities and wellness programs.

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