{"id":2490357,"url":"https://alion.io/job/fortrea-senior-clinical-data-manager-2","title":"Senior Clinical Data Manager","company":{"id":3171,"name":"Fortrea","domain":"fortrea.com","url":"https://alion.io/company/fortrea","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":82,"open_postings":32,"ghost_share":0,"stale_share":0.938,"repost_share":0,"time_to_fill_p50_days":15,"computed_at":"2026-10-29T05:49:05Z"}},"role":"HR","role_family":"HR","seniority":"lead","employment_type":"full_time","work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Beijing, China","Shanghai, China"],"countries":["CN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":8,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false}],"status":"live","first_seen_at":"2026-10-14T01:59:34Z","employer_posted_date":"2026-10-14","last_verified_at":"2026-10-29T20:45:41Z","board_verified":true,"closed_at":null,"days_open":15,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":15},"description":"Fortrea is currently recruiting for an FSP Lead Data Manager for a global pharmaceutical project. This position can be based in either Beijing or Shanghai.\nKey Responsibilities\nVery strong subject matter expertise in the Data Management (DM) discipline. Can support multiple studies concurrently with little to no oversight by functional manager.\nAdvocates the DM position on technical processes within study team meetings. Shares DM process knowledge with study team colleagues and cross functional peers.\nOversees multiple DM vendors and provides training and subject matter expertise to lower-level DM peers.\nLeads by example by providing data management expertise and input into drug development programs.\nMay act as a functional DM expert for a specific DM specialty area, such as data standards, Medical Coding, eSource, external data, data visualization and analytics, etc.\nReview Key Risk Indicators (KRIs) outputs in aggregate across sites, regions and countries. As needed, review study level operational and patient data to support the investigation and root cause analysis of observations.\nSupport the team in assessment of centralized monitoring observations to identify potential issues and risks occurring during study conduct.\nPerforms vendor oversight activities across multiple studies. Reviews and gives input in vendor oversight processes. Proactively shares and provides suggestions on how to improve vendor oversight. Uses metrics and key performance indicators (KPIs) to monitor vendor performance.\nDocuments any process related deviations and communicates to functional manager. Triggers discussion or takes immediate action if there are concerns with respect to quality of DM deliverables.\nExpert cross-functional understanding on the impact of data management processes to other stakeholders.\nLeads the data review meetings for all data sources with Medical, Clinical Operations, Biostatistics, and Programming to highlight and discuss deviations to the protocol and specific data values relevant for the analysis/determining subject populations.\nStrong understanding of regulatory requirements, such as GCP, and how they impact Data Management activities and outputs.\nRequired Qualifications\nBachelor’s degree in biological science, health-related or computer science field (or equivalent experience).\nTypically 8+ years of relevant experience in pharmaceutical, clinical research, or health services industry, including at least 6 years as a Data Manager with progressive leadership responsibility.\nDemonstrated expertise in Data Management from program inception through regulatory submission (regulatory submissions experience preferred).\nRecognized leadership and subject matter expertise in Data Management related global process improvement initiatives.\nExtensive experience with external data management and digital health solutions (e.g., eSource, eCOA, eConsent), including edata processes, central monitoring tools, and risk-based quality management (RBQM) principles.\nAdvanced understanding of clinical data standards (e.g., CDISC) and ability to apply standards across studies and programs.\nStrong computer skills including database management software, reporting tools, and medical coding systems.\nIn-depth knowledge of different data sources in clinical trial settings and associated data quality considerations.\nPrior inspection and audit experience.\nProven project management and organizational skills to prioritize and direct work for self and others to meet timelines.\nAbility to influence and guide study teams, driving decision making and issue resolution across functions and vendors.\nDemonstrated critical thinking and sound judgement in complex or ambiguous data management scenarios.\nDemonstrated learning agility and ability to drive adoption of new technologies and capabilities for Data Management.\nPreferred Qualifications\nSCDM Certificated Clinical Data Manager\nExperience with RAVE, eClinical Solutions elluminate and CluePoints is a plus.\nLearn more about our EEO & Accommodations request here.","description_format":"text","description_chars":4052,"description_truncated":false,"requirements":{"experience_years_min":8,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[{"name":"China","iso":"CN","kind":"country"}],"hiring_excludes":[],"relocation_offered":false,"industries":["Clinical Trial Services 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