Arbetsbeskrivning

Are you passionate about science and have extensive knowledge within the pharmaceutical industry? Are you also experienced in clinical operations and project management? We are now recruiting a Global Clinical Operations Program Director (GPD) to the BioPharmaceuticals Clinical Operations function for Late-Stage Development Cardiovascular, Renal and Metabolic therapy area in R&D to support our vibrant portfolio. This role will be based at AstraZeneca's dynamic R&D site in Gothenburg (SE). The role of a GPD requires global collaboration and leadership. The span of responsibilities is broad and may support one or several products depending on their size and complexity. The products supported will be in Phase 3 development or already commercially available, but the program may include studies in all phases of drug development. This position will focus on projects in the metabolic space, e.g. weight management. The GPD is responsible for oversight of a program of global studies, covering all clinical development deliverables (including aspects of quality, budget, time, resource and risk). The role also involves integrating design, feasibility, and operational planning to ensure clinical drug development programs are aligned with priorities and strategy. The GPD will provide input and support to the Senior GPD in preparation for governance interactions. The GPD may act as the lead for cross-functional teams in delivery of clinical activities assigned. Accountabilities: As a GPD, you will be leading cross-functional teams of experts in the planning and delivery of a defined clinical program of studies and/or clinical activities to scope, quality, budget, time; managing resources and risk on behalf of the Senior GPD. The GPD may manage improvement or change projects within clinical operations or span multiple business areas. You will be an early adopter of new ways of working and acting as ambassador for change when leading teams, also embracing artificial intelligence. The role includes leadership and project management of non-drug project work, e.g. functional and cross-functional improvement initiatives, and you will also contribute to initiatives as Subject Matter Expert. In the role of GPD, you are expected to be able to work independently and be comfortable prioritizing the work for yourself and your team to meet business objectives. You will also mentor and support people's development as appropriate. Essential Skills/Experience: * University degree, preferably in medical or biological sciences or discipline associated with clinical research (Advanced degree is preferred) * At least 10 years' experience from within the pharmaceutical industry or similar large multinational organization * At least 8 years' experience of clinical development / drug development process in various phases of development and therapy areas * Proven knowledge of Clinical operations in the metabolic space, e.g. weight management, especially of investment decisions and clinical trial program design development, including governance interactions. Experience in planning, start-up, and oversight of clinical trials. * Proven knowledge of project management tools and processes * Experience from leading clinical projects and deliverables or similar expertise from other areas of drug development (such as pharmaceutical development). * Proven leadership promoting motivation and empowerment of others to accomplish individual, team and organizational objectives * Skilled & experienced in change management * Ability to look for, and champion, more efficient and effective methods/processes of delivering Clinical Development focusing on key performance metrics around reliability, productivity, cost and quality * Excellent written and verbal communication skills in English * Excellent negotiation, collaboration and interpersonal skills with ability to work effectively with others at all levels of the organization * Demonstrated ability to set and manage priorities, resources, performance targets and project initiatives in a regional and local environment * Integrity and high ethical standards * Adaptability Desirable Skills/Experience: * Project management certification is desirable but not mandatory * Regulatory submission experience * Ability to mentor, develop and educate staff At AstraZeneca, we are committed to making a difference by fusing data and technology with the latest scientific innovations to achieve breakthroughs. Our inclusive environment encourages collaboration with academia, biotechs, and industry partners to create the greatest impact on disease. We harness digital, data science & AI to fast-forward our research, ensuring that our work born in a lab can make a real difference in patients' lives across the world. Join us on this exciting journey! Apply now to be part of a team that makes a bigger impact on patients' lives. So, what's next? We welcome your application, no later than 15 Feb 2026. We will review applications and interview suitable candidates on an ongoing basis.