{"id":3147650,"url":"https://alion.io/job/johnson-johnson-associate-director-safety-analysis-scientist","title":"Associate Director, Safety Analysis Scientist","company":{"id":14152,"name":"Johnson & Johnson","domain":"jnj.com","url":"https://alion.io/company/jnj","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":84,"open_postings":31,"ghost_share":0,"stale_share":0.839,"repost_share":0,"time_to_fill_p50_days":7,"computed_at":"2026-10-24T06:02:35Z"}},"role":"Science & Research","role_family":"Science & Research","seniority":"head","employment_type":"full_time","work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["High Wycombe, United Kingdom"],"countries":["GB"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":123000,"max_usd":234000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":487},"experience_years_min":11,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"SAS","optional":false}],"status":"live","first_seen_at":"2026-10-06T00:00:00Z","employer_posted_date":"2026-10-06","last_verified_at":"2026-10-24T05:46:21Z","board_verified":true,"closed_at":null,"days_open":18,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":18},"description":"At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.\nAs guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.\nJob Function:\nProduct SafetyJob Sub Function:\nProduct Safety Risk ManagementJob Category:\nScientific/TechnologyAll Job Posting Locations:\nHigh Wycombe, Buckinghamshire, United KingdomJob Description:\nAbout Innovative Medicine\nOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.\nJoin us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.\nLearn more at https://www.jnj.com/innovative-medicine\nAbout Oncology\nOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.\nOur Oncology team is focused on the elimination of cancer by discovering new pathways and modalities for finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results.\nJoin us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.\nLearn more at https://www.jnj.com/innovative-medicine\nPlease note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):\nUnited States - Requisition Number: R-059752\nBelgium - Requisition Number: R-062304\nRemember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.\nWe are searching for the best talent for an Associate Director, Safety Analysis Scientist, located in High Wycombe, United Kingdom. This is a hybrid position that requires you to be on site three days a week.\nPurpose:\nThe Associate Director (AD) Safety Analysis Scientist (SAS) provides scientific expertise and leads the safety assessment of assigned products. The AD SAS, in partnership with the Medical Safety Officer (MSO), is responsible for the preparation of scientific safety analysis and evaluations, which are required for regulatory compliance and to aid in safety-related decisions for marketed products and products in development.\nThe AD SAS will support product Safety Management Teams (SMTs) and work in close collaboration with other cross-functional safety partners to determine a product’s safety strategy, complete safety analyses and evaluations, proactively review safety data/lead safety data review meetings and interpret safety information to make a recommendation, supporting SMT deliverables as required.\nThe AD SAS will assist the Medical Safety Officer (MSO) with activities related to the SMT and with contributions to key safety and clinical documents.\nThe AD SAS will have in-depth product knowledge, will serve as product point of contact, and will provide training to, and oversight of deliverables prepared by, other team members as needed (for complex reports).\nThe AD SAS will function with a high level of independence, with minimal guidance from the Director, Safety Analysis Scientist (SAS) Therapeutic Area Lead (TAL), be able to link discussions to content, and consistently deliver high quality results with minimal guidance.\nThe AD SAS will quickly build alliances and be able to independently influence other safety partners to shape strong decisions/outcomes.\nYou will be responsible for:\nLead safety evaluations including strategy discussions, collaborating with Therapeutic Area Safety Head (TASH)/MSO and other stakeholders as necessary, data retrieval, data analysis, report writing, and report revision.\nEnsure high quality safety evaluations and reports with minimal comments from stakeholders and minimal revisions required.\nProvide input and review of key regulatory or clinical documents as appropriate.\nDemonstrate leadership in the SMT and support the MSO.\nSupport SMT activities (e.g., preparing and presenting data, compiling meeting minutes, updating signal tracking information).\nLead proactive safety data reviews, if applicable and form a safety position across Global Medical Safety (GMS) which can be leveraged for aggregate safety reports.\nProvide support for Health Authority interactions regarding safety and risk management, both written and verbal.\nAssume responsibility for novel projects, create value and innovate without defined processes. May seek guidance from Directors (i.e., SAS TAL) for complex projects.\nLead cross-functional training of relevant stakeholders.\nAct as product or process Subject Matter Expert (SME) for audits/inspections.\nParticipate in, or lead, department and/or cross-functional initiatives.\nExplore innovative ways of presenting data, preparing reports, and improving efficiencies within the programs they own.\nAssist Directors in the creation, review and implementation of controlled documents and other related tools.\nManagement of unscheduled reports within the Aggregate Report Calendar.\nManagement activities within smaller Therapeutic Areas, as applicable.\nLine-management of contractor positions within the team, as applicable.\nAct as backup to TAL as needed (e.g., Director SAS TAL is unavailable).\nOversight of deliverables by other team members (e.g., complex reports), as needed\nQualifications / Requirements:\nEducation:\nBachelor’s Degree Required: Healthcare-related or Biomedical Science (11+ years industry experience or equivalent).\nAdvanced Degree Preferred: Healthcare-related or Biomedical Science (8+ years industry\nexperience or equivalent).\nExperience\nRequired:\nMedical writing or Pharmacovigilance (PV) experience required.\nWorking knowledge of medical concepts and familiarity with safety activities in drug development and post marketing and global safety health authority requirements.\nAbility to understand and analyze complex medical-scientific data from a broad range of disciplines.\nAbility to interpret and present complex data to determine benefit-risk impact.\nExcellent English verbal and written communication skills.\nAbility to effectively interact with stakeholders, including business partners.\nAbility to work in a matrix environment, proven leadership skills.\nAbility to plan work to meet deadlines and effectively handle multiple priorities.\nProficiency in Microsoft applications (e.g., Word, Excel, and PowerPoint).\nAbility to independently influence, negotiate and communicate with both internal and external customers.\nPreferred:\nClinical experience preferred.\nOncology experience preferred.\nRequired Skills:\nPreferred Skills:\nClinical Operations, Compliance Management, Compliance Risk, Data Reporting, Medicines and Device Development and Regulation, Mentorship, Presentation Design, Quality Control (QC), Research Ethics, Researching, Risk Management, Safety Investigations, Safety-Oriented, Serious Adverse Event Reporting, Standard Operating Procedure (SOP), Tactical Planning, Technical Credibility, Technical Writing","description_format":"text","description_chars":8013,"description_truncated":false,"requirements":{"experience_years_min":11,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[{"language":"English","level":"All 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