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Clinical Data Manager

Peopleforce Recruitment Ltd

Witney

Hybrid

GBP 40,000 - 60,000

15 days ago

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Job summary

An established industry player is seeking a Senior Data Management Analyst II to join their team in Witney. This role is ideal for an experienced clinical data analyst ready to take the next step in their career. You will collaborate with clinical study teams, manage data systems, and ensure compliance with regulatory standards. With a focus on clinical trials, this position offers the chance to make a significant impact while working in a supportive environment. If you have a degree in a relevant scientific subject and at least 4 years of experience, this could be the perfect opportunity for you to advance your career.

Qualifications

  • 4+ years of experience in clinical data analysis within the UK.
  • Degree qualification in a relevant scientific field.

Responsibilities

  • Collaborate with teams to prioritize tasks and meet study goals.
  • Design/review CRFs and manage data systems for clinical studies.

Skills

Clinical Data Analysis

Regulatory Compliance

Database Management

Team Collaboration

Education

Degree in a relevant scientific subject

Tools

Clinical Trial Management Systems

Job description

Senior Data Management Analyst II
Witney
Initial 12 month contract to be made permanent for the right candidate
1 day WFH per week

We are looking for an experienced clinical data analyst looking to take the next step in their career. This opportunity is perfect for someone with key knowledge within clinical trials or similar technicalities looking to embrace and embark on a new challenge.

General Duties:
  1. Collaborate with clinical study teams and other departments to prioritise tasks, allocate resources, and meet goals.
  2. Support clinical studies by designing/reviewing CRFs, building/validating databases, creating data management documents, and managing laptop setups. Monitor tasks and metrics, providing status reports.
  3. Establish, maintain, and advise on data systems for tracking study progress, providing feedback to teams as needed.
  4. Review and update practices, ensuring compliance with regulatory standards. Contribute to procedure and guideline improvements.
  5. Ensure compliance with Corporate and Divisional Policies and perform additional duties as assigned.
Key Accountabilities and Expectations:
  1. Degree qualification within a relevant scientific subject.
  2. Minimum of 4 years experience within a relevant field within the UK in order to understand UK regulations.
  3. Commutable distance to Witney as well as a right to work within the UK (there is no possibility of sponsorship with this role).
  4. Ability to work collaboratively as a team as well as comfortably independently.

If this seems like the opportunity for you, please feel free to apply or reach out to Maisy at Peopleforce Recruitment.

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