{"id":3387445,"url":"https://alion.io/job/clinchoice-senior-scientist-aggregate-reporting","title":"Senior Scientist - Aggregate Reporting","company":{"id":672996,"name":"ClinChoice","domain":"clinchoice.com","url":"https://alion.io/company/clinchoice","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Greenhouse","truth_index":{"grade":"B","score":78,"open_postings":12,"ghost_share":0,"stale_share":0.833,"repost_share":0.083,"time_to_fill_p50_days":39,"computed_at":"2026-10-28T05:59:10Z"}},"role":"Science & Research","role_family":"Science & Research","seniority":"senior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Bengaluru, India"],"countries":["IN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":17000,"max_usd":39000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":1296},"experience_years_min":8,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-10-28T05:13:45Z","employer_posted_date":"2026-10-28","last_verified_at":"2026-10-28T21:14:13Z","board_verified":true,"closed_at":null,"days_open":0,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":0},"description":"Responsibilities:\nThe Pharmacovigilance Medical Safety Scientist is responsible for developing, reviewing, and maintaining high-quality safety and pharmacovigilance documents that support the safety surveillance and regulatory compliance of consumer health products.\nThis role requires the ability to synthesize data from multiple sources, including individual case safety reports (ICSRs), aggregate safety data, clinical studies, epidemiological research, literature reviews, post-marketing surveillance, signal detection activities, and other safety data sources. The successful candidate will transform complex safety information into clear, concise, and scientifically accurate documents that support global pharmacovigilance activities and regulatory submissions.\nThe individual will work closely with Drug Safety, Medical Affairs, Regulatory Affairs, Clinical Development, Quality, and R&D teams to ensure consistent, evidence-based communication of product safety information.\nThis is an individual contributor role with no direct reports.\nKey responsibilities include, but are not limited to:\nPharmacovigilance and Medical Writing:\nPrepare, review, and maintain pharmacovigilance and risk management documents for consumer health products. \nSynthesize safety information from multiple sources, including:\nIndividual Case Safety Reports (ICSRs)\nAggregate safety data analyses\nClinical trial safety data\nPost-marketing surveillance data\nEpidemiology studies\nPublished literature\nSignal detection and evaluation activities\nBenefit-risk assessments\nHealth Authority Assessment Reports\nDraft and support the preparation of:\nPeriodic Safety Update Reports (PSURs/PBRERs/PADERs)\nAd Hoc Safety Reports\nDevelopment Safety Update Reports (DSURs) \nSignal assessment reports\nAggregate safety reports\nRisk management documentation\nHealth authority responses\nSafety narratives\nSafety sections of regulatory submissions\nSafety surveillance reports and presentations\nAnalysis and evaluation for the Safety Management Teams (SMT)\nSafety Data Analysis and Interpretation\nCollaborate with Safety Scientists, Medical Reviewers and others to evaluate emerging safety information and communicate findings effectively.\nAssist in the interpretation of safety trends, potential signals, and benefit-risk considerations.\nSupport literature surveillance activities and summarize relevant safety findings.\nContribute to the development of safety conclusions and evidence-based recommendations.\nSupport the preparation, review, and analysis of risk management activities and reports.\nQuality and Compliance\nEnsure all documents comply with global pharmacovigilance regulations, company SOPs, and applicable guidance documents.\nMaintain high standards of scientific accuracy, consistency, grammar, and document quality.\nPerform quality control reviews of safety documents and ensure timely delivery of assigned projects.\nSupport inspection and audit readiness activities through accurate documentation practices. \nEducation/Experience: \nAdvanced degree required: PharmD, PhD, MD, MPH, MS, or equivalent scientific discipline.\n8-10 years of experience in pharmacovigilance, drug safety, medical writing, regulatory writing, or related pharmaceutical, consumer health, or medical device industries.\nExperience preparing safety and pharmacovigilance documents preferred.\nFamiliarity with global pharmacovigilance regulations and safety reporting requirements.\nExperience working in a matrixed environment with multiple stakeholders. \nTechnical Competencies\nStrong understanding of:\nClinical research methodologies\nEpidemiology and biostatistics\nEvidence-based medicine\nRegulatory and scientific communication requirements\nSafety and benefit-risk assessment principles\n2. Expertise in literature evaluation and scientific data interpretation. \n3. Ability to critically analyze multiple complex scientific information and identify key insights to drive product safety. \nSkills:\nExcellent medical writing, editing, and proofreading skills.\nExceptional grammar, attention to detail, and document quality standards.\nStrong analytical and critical thinking capabilities.\nEffective project management and organizational skills.\nStrong verbal and written communication skills.\nAbility to work independently while managing multiple priorities and deadlines.","description_format":"text","description_chars":4323,"description_truncated":false,"requirements":{"experience_years_min":8,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"phd","optional":false},"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Clinical Trial Services (CRO)"],"lifecycle":[{"event":"open","at":"2026-10-28T08:22:42Z"}],"visa":[],"liveness":{"score":86,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.86,"p_room":1,"age_days":0,"expected_fill_days":39,"reasons":["conf:3","win:early"],"computed_at":"2026-10-29T01:07:41Z"},"pay":null,"html_url":"https://alion.io/job/clinchoice-senior-scientist-aggregate-reporting","json_url":"https://alion.io/job/clinchoice-senior-scientist-aggregate-reporting.json","meta":{"generated_at":"2026-10-29T01:07:41Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":1591,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-10-30T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.02,"usd":0.002,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":672996},"rest":"https://alion.io/mcp/rest/get_company?id=672996"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fclinchoice-senior-scientist-aggregate-reporting"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":1,"usd":0.1},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Fclinchoice-senior-scientist-aggregate-reporting"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.02,"usd":0.002},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Fclinchoice-senior-scientist-aggregate-reporting"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/clinchoice-senior-scientist-aggregate-reporting\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fclinchoice-senior-scientist-aggregate-reporting"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":3387445}},{"tool":"search_jobs","arguments":{"company":"clinchoice.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":3387445},"note":"people open to offers who fit this vacancy"}],"note":"The same data through MCP tools: https://alion.io/mcp/open needs no sign-in (compact searches, postings, people); https://alion.io/mcp with an Alion account has everything. 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