Job Title – Associate Director, Clinical Research Contract Length – ASAP until end of May 2026

Key Responsibilities

Provide appropriate scientific/technical contribution or author the clinical development plan for the studies/projects assigned. With support from Clinical Research Director design fit-for-purpose clinical strategies and other clinical evidence generation strategies to support the business for innovation product/therapy area including medical devices, in line with ICH GCP and other regulatory requirements (as needed). Support peer review publications/input to clinical section of regulatory dossiers to ensure that they are scientifically robust from a medical and scientific standpoint. Responsible for the design, implementation, reporting, interpretation, disclosure and publication of company sponsored clinical studies to ensure these follow external e.g. GCP, internal Medical Governance and other internal policy requirements. Responsible for contributing clinical content to regulatory submissions and other regulatory engagements for clinical research activities. Responsible for supporting clinical/medical due diligence for external opportunities from a clinical research point of view.