Job Description

We are partnering with a global biopharmaceutical organisation to appoint a Clinical Scientist to support drug development programs within a dynamic, cross-functional clinical team. This role offers the opportunity to work closely with internal scientists, clinical operations, and regulatory stakeholders, contributing directly to the design, execution, and communication of clinical studies.

Key ResponsibilitiesSupport clinical study design and development , including contribution to protocols, ICFs, and associated clinical documentationReview, prepare, and support regulatory documents in line with EMA and local authority requirementsCollaborate closely with clinical scientists and study teams on study follow-up, data review, and scientific analysisContribute to clinical writing activities , including study reports, abstracts, posters, publications, and congress communicationsSupport cross-functional teams throughout the clinical trial lifecycle, ensuring quality, compliance, ...

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