Join us as a Global Study Associate Director (GSAD) in our BioPharmaceuticals Clinical Operations team at AstraZeneca's dynamic R&D site in Gothenburg (Sweden). This role is pivotal in the delivery of clinical studies, providing direction and guidance to a cross-functional study team within the Cardiovascular, Renal and Metabolism (CVRM) therapy area. As the main liaison between the study team and the Clinical Program Team (CPT), you will be accountable for the delivery of a study according to agreed timelines, budget, and quality standards. AccountabilitiesAs a GSAD, you will lead and provide guidance to a cross-functional study team, ensuring the clinical study progresses as planned. You will be responsible for developing essential study level documents, overseeing external service providers, and ensuring all systems used at a study-level are current and accurate. You will also oversee study level performance against agreed upon plans, milestones, and key performance indicators. Additionally, you will be responsible for study budget re-forecasting and management throughout the study lifecycle. Essential Skills/ExperienceUniversity degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical researchRelevant clinical experience in the pharmaceutical industry, including project management experienceExtensive study management experienceExtensive knowledge of ICH-GCP, clinical research regulatory requirementsDemonstrated solid project management skillsStrong abilities in team leadership with experience from cross-functional leadership of a clinical study or part of a clinical studyExcellent communication and interpersonal skillsStrong strategic and critical thinking abilitiesAbility to manage competing priorities Desirabl…Forskare, farmakologiFarmakologer och biomedicinare
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