{"id":2170734,"url":"https://alion.io/job/parexel-data-surveillance-analyst-based-in-selected-emea-locations-2","title":"Data Surveillance Analyst - based in selected EMEA locations","company":{"id":2735,"name":"Parexel","domain":"parexel.com","url":"https://alion.io/company/parexel","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":83,"open_postings":43,"ghost_share":0,"stale_share":0.884,"repost_share":0,"time_to_fill_p50_days":17,"computed_at":"2026-11-03T05:54:40Z"}},"role":"Analytics","role_family":"Analytics","seniority":null,"employment_type":null,"work_mode":"remote","remote_scope":"stated_regions","remote_scope_basis":"posting_text","remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["Bloemfontein, South Africa","Croatia","Hungary","Czech Republic","Lithuania","Poland","Serbia","Romania"],"countries":["ZA","HR","HU","CZ","LT","PL","RS","RO"],"hiring_countries":["DE","FR","AE","GB","AT","BE","BA","BG","HR","CY","CZ","DK","FI","HU","IE","IL","IT","KE","ME","NL","NG","NO","PL","RO","SA","RS","ZA","ES","SE","CH","TR","UA","AL","DZ","AD","AO","BH","BJ","BW","BF"],"hiring_countries_total":116,"salary":null,"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CDISC","optional":false},{"name":"Microsoft Office","optional":false},{"name":"SAS","optional":false},{"name":"SQL","optional":false}],"status":"live","first_seen_at":"2026-09-12T00:00:00Z","employer_posted_date":"2026-10-15","last_verified_at":"2026-11-03T07:12:18Z","board_verified":true,"closed_at":null,"days_open":52,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":52},"description":"When our values align, there's no limit to what we can achieve.\nAt Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.\nEach of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.\nThis home-based position is available to candidates in selected EMEA locations. Applicants must be based in one of the eligible locations.\nPicture Yourself At Parexel:\nThe Data Surveillance Analyst (DSA) is responsible for analyzing scientific and operational data to support the Data Surveillance process and reviewing project-specific Quality Tolerance Limits. They assist in developing Data Surveillance Plans (DSPs) and conduct defined project reviews. The DSA also attends internal and external Data Surveillance meetings, where they present relevant findings to the project team.\nWhat You'll Do At Parexel:\nData Surveillance Plan Development and Technology Configuration:\nSupport the development of a robust Data Surveillance Plan, including Key Risk Indicators, Quality Tolerance Limits, and central statistical analysis.\nConfigure and Maintain Data Surveillance technologies (e.g., CluePoints Central Monitoring Platform): create data import mapping for all data sources; create and set-up standard and bespoke KRIs; create and set-up statistical analysis parameters.\nData Surveillance Review:\nReview relevant data via the scoped technologies and additional sources as required to support reviews designated for the DS Analyst per the project specific Data Surveillance Plan, including project specific Quality Tolerance Limits.\nDocument findings from Data Surveillance activities in the DS Findings Form, Issue Tracking system(s) and other as appropriate.\nProvide feedback and work with Technology teams to identify potential solutions that match the business and technology strategy.\nApply working knowledge and judgment to identify and evaluate potential data quality trend, outliers and emergent issues. Determine and implement appropriate follow-up action with the input of other / relevant parties and / or guidance provided, if applicable.\nActively participate in Investigator and other external or internal meetings and audits & regulatory inspections as required.\nRecognize impact of study non-compliance/issues/delays/data quality signals and communicate/ promptly escalate to FL any site and/or study issues that require immediate action.\nPerform core reviews per DS Plan.\nDocument instances of atypical data per DS Plan.\nCollaborate with DS Team Members to correlate findings from various sources.\nSupport Project Leads with DS Review meeting, driving reviews and decisions as needed and agreeing on actions.\nEngage DS Team to compile signals/actions into client ready list.\nSupport documentation of actions in CluePoints Issue Management system (links to IH for any on-site interventions required).\nComplete, share, and file Central Monitoring Report.\nHere are a few requirements specific to this advertised role:\nUniversity degree (medical, biological science, pharmacy, and/or data analytics).\nFluent English.\n Hands-on programming experience in SAS, R, and/or SQL is a must-have.\nExperience with Risk-Based Quality Management (RBQM) processes and data surveillance methods.\nFamiliarity with centralized monitoring and Data Driven Monitoring practices.\nProficient in data analysis, trend identification, and issue triage.\nProficient in relevant software: CTMS, EDMS, MS Office.\nBasic understanding of SDTM domains and data operations concepts.\nExperience with CluePoints would be a strong asset.\nClient-focused with strong quality orientation.\nEffective in matrix and global virtual team environments.\nExcellent interpersonal and communication skills, including presentation abilities.\nStrong time management and multitasking capabilities.\nAbility to work independently with minimal supervision.\nWhy join us:\nBe part of groundbreaking projects that are pushing the boundaries of the industry. 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