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    • Support the UK RPP in maintaining an effective pharmacovigilance system in compliance with MHRA requirements.
    • Assist in ensuring continuous oversight of all PV…
    • Understands the clinical impact of antibody and multi-specific-based therapies.
    • Liaise with Therapy area leaders and the drug pipeline-focused teams to identify…
    • Supporting clinical assessment projects within key hospital accounts.
    • Supporting product evaluations, trials and implementation activities.
    • Develop new vitro models and pre-clinical activities to explore efficacy of new ImmTAAI effector molecules.
    • To conduct and design experimental investigations…
    • In-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical data management,…
    • In case of clinical emergency or major incident, the actions of the Switchboard Operator contribute to ensuring that all relevant clinical and operational…
    • Technical Mastery: Extensive understanding of end-to-end pharmacovigilance processes, including Deviation/CAPA management and the conduct of clinical research.
    • Assist in clinical trial support when required.
    • Ensure compliance with clinical and safety protocols.
    • Provide clinical insights to the commercial team to shape…
    • Design and run global real-world evidence (RWE) studies from concept through to publication.
    • Work on a collaborative study with an academic partner to grow a…
    • Provide highly specialised clinical advice to the pharmacy clinical trials team regarding haematology and oncology trials conducted within the Trust.
    • Extensive technical pharmacy production experience, including GMP, clinical trials, and chemotherapy services.
    • Job Types: Full-time, Part-time, Temporary.
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    • Knowledge of the pharmaceutical, biotechnology, and/or clinical trial industry.
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    • Experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements.
    • At least 3 years of experience or understanding of clinical study start-up requirements and activities, showing your expertise in the field.