About the Role
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 Responsibilities
Support clinical study design and development, including contribution to protocols, ICFs, and associated clinical documentation
Review, prepare, and support regulatory documents in line with EMA and local authority requirements
Collaborate closely with clinical scientists and study teams on study follow-up, data review, and scientific analysis
Contribute to clinical writing activities, including study reports, abstracts, posters, publications, and congress communications
Support cross-functional teams throughout the clinical trial lifecy...
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 Responsibilities
Support clinical study design and development, including contribution to protocols, ICFs, and associated clinical documentation
Review, prepare, and support regulatory documents in line with EMA and local authority requirements
Collaborate closely with clinical scientists and study teams on study follow-up, data review, and scientific analysis
Contribute to clinical writing activities, including study reports, abstracts, posters, publications, and congress communications
Support cross-functional teams throughout the clinical trial lifecy...
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