Clinical Data Insights Scientist I

WillHire

Dublin

Hybrid

EUR 83,000 - 138,000

Full time

14 days+

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Job summary

Novartis, in partnership with Magnit Global, seeks a Clinical Scientific Expert I (CSE External/Contractor) to provide clinical data review and insights across study phases. You will ensure data quality, support safety analytics, and collaborate with the Integrated Clinical Trial Team (iCTT).

This temporary role offers a hybrid work arrangement and training support. The ideal candidate holds an advanced life sciences degree with 1–2 years (or 3–4 years in related Clinical Operations) experience,

Qualifications

  • Advanced life sciences/healthcare degree required; Master’s or PhD strongly preferred.
  • 1-2 years scientific/operational experience in planning, executing, reporting clinical studies, or 3-4 years in Clinical Operations/Clinical Science.
  • Good knowledge of GCP and drug development processes.
  • Strong scientific knowledge in at least one therapeutic area.
  • Knowledge of data collection/reporting systems (Rave/OC-RDC advantageous).
  • Analytical background with ability to detect data trends and elevate as needed.
  • Fluent English (oral and written).

Responsibilities

  • Ensure high-quality clinical data review and insights through the iCTT.
  • Contribute to data review/quality plans and study data integrity.
  • Support CRF development and data capture tool implementation.
  • Assist in data review process improvements and pharmacovigilance activities as needed.
  • Attend study-level meetings as required.

Skills

Clinical data review
ICH GCP knowledge
Statistical analysis
Medical writing
English fluency

Education

Advanced life sciences degree
Master’s/PhD preferred

Tools

Rave
OC-RDC
EDC systems
Excel

Job description

Novartis, in partnership with Magnit Global, seeks a Clinical Scientific Expert I (CSE External/Contractor) to provide clinical data review and insights across study phases. You will ensure data quality, support safety analytics, and collaborate with the Integrated Clinical Trial Team (iCTT).

This temporary role offers a hybrid work arrangement and training support. The ideal candidate holds an advanced life sciences degree with 1–2 years (or 3–4 years in related Clinical Operations) experience,

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