{"id":444227,"url":"https://alion.io/job/astrazeneca-safety-physician-ta-lead-oncology","title":"Safety Physician TA Lead - Oncology","company":{"id":13195,"name":"AstraZeneca","domain":"astrazeneca.com","url":"https://alion.io/company/astra-zeneca","size_band":"1001-5000","is_staffing_agency":false,"is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":90,"open_postings":95,"ghost_share":0,"stale_share":0.6,"repost_share":0.011,"time_to_fill_p50_days":14,"computed_at":"2026-09-24T05:45:00Z"}},"role":"Finance","role_family":"Finance","seniority":"lead","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Shanghai, China"],"countries":["CN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":10,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-07-31T00:00:00Z","employer_posted_date":"2026-07-31","last_verified_at":"2026-09-24T15:37:29Z","board_verified":true,"closed_at":null,"days_open":55,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":55},"description":"Typical Accountabilities:\nSafety Governance and Risk Management Activities (30%)\nBe responsible for the development and implementation of China Clinical Safety strategy for assigned projects and products throughout all stages of development, and ensure CN alignment for Project Specific Safety Requirements (PSSR).\nRepresents PS on cross-functional Clinical Teams and/or Project Teams for developmental and/or marketed products.\nBe responsible for the development of LRMPs, collaborate with MC PV physicians and key stakeholders to ensured aRMM/aPV aligned in final LRMPs\nProvides medical input to ensuring that risk-minimisation strategies are implemented appropriately in relevant documents such as product reference safety information.\nProvides strategic clinical safety input into Clinical Development planning activities.\nProvides strategic and medical input to project specific safety requirements. Reviews and provides technical input and approval for protocols, informed consents, clinical study reports and safety relevant content of clinical technical documents as appropriate.\nSets strategic direction for addressing safety issues in regulatory submission and communication/interaction\nProvides input on cross-functional ad-hoc teams set up to address urgent and important safety issues.\nSignal Detection, Evaluation and Labelling (10%)\nCollaborates with global PS in safety surveillance activities including but not limited to medical review of ICSR, signal detection and evaluation , activities relevant to Safety Information Review Committee (SIRC);\nProvides medical input to regulatory supporting documentation for labelling updates.\nProvides medical input into Identification and utilization of appropriate sources of information and database searches to retrieve relevant data for evaluation of signals.\nCollaborates in routine signal management activities.\nProvides medical input to deliver accurate and fit for purpose safety evaluation documents with clear conclusions in response to internal or regulatory authority requests for safety data.\nProvides strategic input into responses to regulatory requests for local label deviations from the company core safety documentation.\nTeam leader (60%)\nOversight of the full disease area product portfolio, and link with local management and key stakeholders.\nIn responsible disease area, collaborate closely with China product teams and corresponding global patient safety teams, develop/implement relevant safety strategies to support product clinical development and lifecycle safety management.\nAccountable for mentoring, performance evaluation and career development of the team members.\nMonitor and forecast team workload to identify, mitigate and escalate potential resource and non-compliance issues.\nSupport the head of safety science team to develop necessary processes and procedures to ensure compliance and efficiency.\nSupport the head of safety science team to collaborate with local and global relevant teams for the update and review of safety related SOPs/guidelines to ensure the compliance with company policies and requirements of health authority.\nEducation, Qualifications, Skills and Experience\nMedical background\nAt least 10 years of Drug Development/Patient Safety experience in MNC\nStrong people management and leadership capabilities\nAdequate understanding of the China and global regulations/guidances in order to have effective oversight of R&D China safety monitoring process\nDrug development experience and good understanding of Clinical Study Process\nGood medical knowledge in AZ Therapeutic Areas.\nExcellence in pharmacovigilance and Patient Benefit risk assessment\nGood organizational skills with the ability to multi-task and prioritize assignments (planning and organizing)\nFluent in written and spoken English\nDate Posted\n31-7月-2026Closing Date\n30-10月-2026AstraZeneca 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.","description_format":"text","description_chars":4477,"description_truncated":false,"requirements":{"experience_years_min":10,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":null,"security_clearance":false,"languages":[{"language":"English","level":"All levels","optional":false}]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Health Care","Pharmaceuticals","Biopharma"],"lifecycle":[{"event":"open","at":"2026-09-06T07:35:53Z"}],"liveness":{"score":10,"band":"cold","label":"Long shot","p_open":1,"p_active":0.354,"p_room":0.28,"age_days":55,"expected_fill_days":14,"reasons":["conf:0","stale_co","velocity","win:tail","crowd:brand"],"computed_at":"2026-09-24T05:45:00Z"},"pay":null,"html_url":"https://alion.io/job/astrazeneca-safety-physician-ta-lead-oncology","json_url":"https://alion.io/job/astrazeneca-safety-physician-ta-lead-oncology.json","meta":{"generated_at":"2026-09-24T19:43:18Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers"}}