Senior Clinical Data Manager — Remote/Late-Phase Lead

Fortrea

United States

Hybrid

GBP 75,000 - 110,000

Full time

8 days ago
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Benefits offered by this job

Remote/hybrid work
Pension contributions
Health insurance
Remote working allowance

Job summary

Fortrea is seeking a Senior Clinical Data Manager to lead data management on late-phase studies. You will act as the technical data management leader across start-up to completion, collaborating with programming, statistics and drug safety to deliver high quality data.

The role offers flexible working arrangements within EMEA, a permanent contract, and ongoing mentoring. You will drive data management plans, QA plans and process improvements while maintaining client satisfaction and meeting

Qualifications

  • A university/college degree in life sciences or related field.
  • Lead experience across late-phase (IIb-III) trials.
  • EDC experience, preferably with RAVE and other EDCs.
  • Excellent oral and written communication and presentation skills.
  • Deep knowledge of clinical trial processes, data management, biometrics and quality management.

Responsibilities

  • Lead data management activities across start-up, maintenance, and completion for projects.
  • Develop global Data Management Plans and QM Plans to ensure high quality data.
  • Identify and implement solutions to data management issues with proactive prevention.
  • Coordinate client liaison and provide data management status, cycle times, and metrics.
  • Collaborate with cross-functional teams to support data management setup, maintenance, and closure.
  • Support process improvements and contribute to project revenue and margins.

Skills

Leadership experience
RAVE experience
EDC experience
Communication skills
Clinical trial knowledge

Education

University/college degree (life sciences)

Tools

RAVE
Other EDC tools

Job description

Fortrea is seeking a Senior Clinical Data Manager to lead data management on late-phase studies. You will act as the technical data management leader across start-up to completion, collaborating with programming, statistics and drug safety to deliver high quality data.

The role offers flexible working arrangements within EMEA, a permanent contract, and ongoing mentoring. You will drive data management plans, QA plans and process improvements while maintaining client satisfaction and meeting

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