Associate Director Patient Safety Scientist

Introduction: 
The Associate Director, Patient Safety Scientist role leads the review of safety data and related documents for potential safety issues in collaboration with the Global Safety Physician (GSP) and (Associate) PV Scientist.  He/she authors and leads PV input to safety documents and regulatory reports. Associate Director, Senior Patient Safety Scientist leads meetings and presents safety data and analyses.

Main Responsibilities:
•    Leads and/or conducts proactive pharmacovigilance and risk management planning for more complex products, including preparation of the safety aspects of Global Risk Management Plans and Risk Evaluation and Mitigation Strategies (REMS) in partnership with the GSP and others as appropriate.  
•    Leads PS activities of cross-functional project teams for developmental compounds and/or marketed products. 
•    Leads and provides safety expertise to Investigator Brochures, Protocols, Informed Consents and Clinical Study Reports. 
•    Has the ability to perform duties as a Safety Strategy and Management Team (SSaMT) Leader for larger or more complex projects.
•    Presents complex issues to Safety Information Review Committee (SIRC) and takes the lead role in data evaluation and discussion of the results with the SIRC Chair, GSP and other key stakeholders. 
•    Leads the collaboration with GSP and Clinical representatives and authors the Reference Safety Information (RSI) for multiple or complex development products.  
•    Authors/provides strategic input or oversight for multiple or complex periodic regulatory documents (PBRERs, PSURs, DSURs) according to the agreed process and timelines. 
•    Authors/provides strategic leadership to regulatory submissions for new products, formulations or indications (NDA/BLA, MAA), in partnership with the GSP and other functional experts.
•    Participates in negotiations and provides expertise to the PS component of contracts/agreements with third parties to ensure quality and integrity of agreements. 
•    Trains and mentors junior members of the team, e.g. in approved PV processes, analytic methodologies, etc. 

You Will Need to Have
•    A life sciences/pharmacy/nursing degree
•    Demonstrated Patient Safety experience including:

•  Clinical drug development (Early and/or Late Phase: program level safety strategy, including proactive risk identification & mitigation planning)
•  Post-Marketing Surveillance (including signal detection & evaluation)
•  Periodic Safety Reports (strategy, preparation and authoring)
•  Risk Management Plans (strategy, preparation and authoring)
•  Knowledge of pharmacovigilance regulation

•    Fluent in written and verbal English
•    Basic understanding of epidemiology

 
AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. 

Date Posted

25-Sep-2025

Closing Date

23-Oct-2025

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.