Scientific Study Leader - BioPharmaceuticals Medical, Cardiovascular, Renal and Metabolism (BPM CVRM)

About this role

Responsibilities

• Scientific Study Leader
• for CVRM, reporting to the CVRM Evidence Strategy Group Director, is leading epidemiology and observational research in close collaboration with the Evidence Strategy Leads as well as the cross-functional study team members with complementary expertise for the successful delivery of studies based on observational research methodologies.
• The role is integral throughout the lifecycle of a drug, from drug discovery and development through commercialization of pharmaceuticals, related the implementation of Evidence strategies in a specific disease area and study planning to generating the evidence required to transform health care and make sure the patients get access to the right medicine in the right time. The evidence needs to fulfil the requirements by the regulators, payers, policy makers, HCPs and patients to facilitate patient access and appropriate use of AZ medicines.
• Major activities include design, initiation, management, conduct, analysis, and reporting of observational studies, including critical appraisal of relevant epidemiological literature and development of medical evidence plans to fill critical knowledge gaps. The role is strategic as well as scientific and involves shaping and executing evidence plans on observational studies aligned with the global medical strategy.
• Typical Accountabilities
• Scientific study leadership in epidemiology and observational research studies, including planning, design, execution, analysis, interpretation, and communication of assigned observational studies, applying relevant epidemiological and analytical methods and ensuring that the studies have relevant quality, are conducted in accordance with written procedures and current legal requirements and internal standards, and fulfil the requirements by the multiple external stakeholders; regulators, payers, policy makers, HCPs and patients to facilitate patient access and appropriate use of AZ medicines
• Scientific Committee coordination and Investigator Management to bring scientific insights and maximize the value of the study while establishing constructive working relationship/interactions with external scientific experts. Promote good research practices, including considerate utilization of emerging methodologies, and technology and represent AstraZeneca’ position when interacting with external experts, collaborative groups, and contract research organizations
• Manage briefing of and facilitate translation of scientific data to relevant messaging for senior leaders and internal stakeholders on assigned study, as applicable and in collaboration with relevant roles
• Active contribution to Evidence strategies and study planning to generate the evidence required to transform health care and make sure the patients get access to the right medicine at the right time.
• Contribute with subject matter expertise in corporate governance procedures for review and approval of medical studies (defined by SOPs) as well as internal trainings

Requirements

• Doctoral level degree (Ph.D. or equivalent) in epidemiology or related health science field and with significant experience (5+ years) in the health care environment, pharmaceutical industry or closely related epidemiological research. Alternatively, an MSc or MPH with substantial experience in the health care environment or equivalent.
• Excellent knowledge in epidemiological methodology and ability to apply it at an international level within the pharmaceutical industry, with hands-on experience of planning, execution, results interpretation and publications, utilizing secondary data and conducting primary data collection studies
• Communication and collaborative skills with the ability to effectively engage and consult with recognized key external scientific experts
• Broad knowledge of healthcare systems and ability to provide proactive and strategic scientific leadership applying emerging methodologies and technologies
• Ability to provide critical appraisal to study designs and published studies
• Work policy:
• When we put people in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office.
• This role is located in Gothenburg, Sweden and is not available for remote work or with travel or commuting support.
• What's next?
• If this sound like the position and place for you - apply today!
• We look forward to receiving your application, but no later than
• April 27, 2026
• . The interview process will be ongoing, so don’t hesitate to apply early.
• Date Posted
• 10-apr.-2026
• Closing Date
• 27-apr.-2026
• Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.