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Clinical Data Manager - homebased (FSP)

Nanosep AB

London

Remote

GBP 50,000 - 70,000

Full time

2 days ago
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Job summary

Nanosep AB seeks a Clinical Data Manager for a homebased role focused on managing complex clinical data reviews within Oncology and CV&M areas. The position requires at least 4 years of relevant experience and prior knowledge of Rave. The successful candidate will support data review throughout the trial process, ensuring compliance and timely delivery of milestones.

Qualifications

  • 4+ years of experience supporting studies in Oncology or CV&M.
  • Experience with low to moderate complexity trials or one high complexity trial.
  • Knowledge of medical terminology preferred.

Responsibilities

  • Providing scientific data review support and managing data flows.
  • Involvement in protocol design and input into data collection tools.
  • Collaborating with trial teams to establish data review expectations.

Skills

Clinical data review
Data management
Oncology experience
Knowledge of medical terminology

Education

BS/BA degree in Health Sciences or related field

Tools

Rave

Job description

Join to apply for the Clinical Data Manager - homebased (FSP) role at Nanosep AB.

Looking for a data management expert with prior experience in performing complex clinical data reviews in close collaboration with Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS).

Requirements include:

  • Extensive experience (4+ years) supporting studies within Oncology or CV&M therapeutic areas.
  • Mandatory Rave experience.
  • Support for low to moderate complexity trials or one high complexity trial.

Key responsibilities include:

  • Providing scientific data review support, managing data flows, and performing continuous data review activities.
  • Involvement from protocol design onwards, providing input into data collection tools.
  • Reviewing scientific study data, managing queries, and leading meetings.
  • Collaborating with trial teams to establish data review expectations, review content, and ensure compliance with regulatory standards.
  • Planning, tracking, and ensuring timely delivery of CDM milestones.

Qualifications:

  • BS/BA degree or higher in Health Sciences or related field.
  • 4 years of data management experience, including clinical data review.
  • Knowledge of medical terminology is preferable.

This role is not eligible for UK visa sponsorship.

IQVIA is a global leader in clinical research services, creating connections to accelerate the development of medical treatments and improve patient outcomes. Learn more at https://jobs.iqvia.com.

We value diverse talent and are committed to innovation and impact. Join us in our mission to improve healthcare worldwide.

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