POSITION SUMMARY
You will provide clinical and scientific support for global Phase 14 vaccine clinical studies within the Vaccines portfolio. Working in close partnership with clinical colleagues, this role contributes to study design, clinical data review, safety oversight, and scientific integrity across assigned studies.
POSITION RESPONSIBILITIES
1. Maintains current scientific and clinical knowledge in the specific disease area(s) of assignment.
2. Supports development of protocols, informed consent documents, and study-level clinical documentation, with oversight from clinical colleagues.
3. Provides input into study set-up activities, including data collection tools, database design considerations, and clinical data outputs.
4. Reviews and queries clinical study data in line with the clinical data review strategy.
5. Reviews, reports, and manages protocol deviations.
6. In partnership with medically qualified colleagues, supports ongoing safety review activities.
7. Contributes to the review of clinical study reports, regulatory responses, publications, and audit or inspection readiness activities.
8. Collaborates effectively with Clinical Operations, Data Management, Statistics, Regulatory, Medical Writing, and external partners (e.g. CROs, vendors) to ensure timely, compliant study delivery.
9. Ensures t...