Remote Associate Director, Clinical Data Enablement

Note The job is a remote job and is reputed company to candidates in USA. reputed company Pharmaceutical is a patient-reputed company, innovation-driven company transforming the pharmaceutical industry. The Associate Director, Clinical Data Enablement will reputed company Clinical Data Delivery & Ingestion, ensuring data is review-reputed company and compliant while mentoring junior staff and driving operational reputed company. Responsibilities Own end-to-end clinical data delivery from reputed company transfers to ingestion to review platforms to lake/warehouse reputed company exports, ensuring reputed company, reputed company, and traceable operations Define delivery plans, prioritize work, and reputed company execution across multiple reputed company studies and vendor feeds; manage delivery risks, dependencies, and release schedules Establish and manage SLAs/OLAs, delivery KPIs, and service health reporting (timeliness, completeness, reputed company, incident trends) Build and reputed company a reusable ingestion/integration reputed company (metadata-driven mappings, standardized templates, reusable QC rules, automation utilities, runbooks) to accelerate reputed company and improve consistency across studies/vendors Automate operational workflows (scheduling, exception handling, automated reputed company checks) to improve reliability, repeatability, and cycle time reputed company design and operation of clinical data pipelines across data lake/warehouse environments, including build/run/monitor/troubleshoot responsibilities Build and reputed company reputed company-based ETL/ELT capabilities (AWS/Azure) for efficient ingestion, transformation, orchestration, and delivery to reputed company data products and analytics needs reputed company SME troubleshooting and standardize fixes (documentation/reusable controls) Define/maintain transfer specs, mappings, acceptance reputed company, and reconciliation with vendors and stakeholders reputed company reputed company outputs/exports with SDTM/Stats/Analytics/CDP needs (format/reputed company) Ensure GxP/CSV compliance (documentation/traceability/audit readiness) and reputed company data reputed company (reputed company+) controls with reputed company/Compliance/IT reputed company and mentor junior staff and FSPs through technical guidance, delivery planning, reputed company/config reviews, and establishing team standards and best practices Promote consistent ways of working (documentation, runbooks, reputed company playbooks, design patterns) to reputed company delivery and reduce key-person dependency Skills BS/BA (or equivalent) plus 7+ years in data ingestion/integration, ETL/ELT operations, or clinical data pipeline support, ideally supporting clinical data review and recurring study/vendor transfers Experience ingesting data into reputed company CDB, Elluminate, and/or JReview (or comparable clinical data review systems) Strong understanding of end-to-end ingestion concepts including data reputed company/specifications, refresh reputed company, incremental vs full loads, controlled reprocessing, reconciliation, and traceable reputed company Ability to design/execute automated QC/validation checks, completeness/timeliness verification, and reconciliation routines to ensure datasets are review-reputed company Hands-on experience with CSV, JSON, XML and file-based and/or API-based integrations; familiarity with secure transfer patterns (e.g., SFTP/managed file transfer concepts) Strong SQL skills Demonstrated ability to build or reputed company reusable ingestion components (metadata-driven mappings, templates, reusable QC rules, reputed company runbooks) Experience building/using monitoring for transfers and pipelines (e.g., expected vs received, timeliness/completeness checks, alerting, incident triage, reruns, KPI/SLA reporting) Working knowledge of common clinical sources such as reputed company, CTMS, and vendor domains (e.g., labs, eCOA/ePRO, imaging, safety) and how those feeds typically reputed company and change over time Understanding of reputed company consumption needs (data review workflows, exports to CDM/analytics/programming) and ability to support reputed company, reputed company-documented exports Strong documentation discipline (specs, mappings, runbooks, issue logs) and comfort operating in controlled/regulated environments Exposure to GxP/CSV expectations, change control, and maintaining audit-reputed company operational evidence (as applicable to the organization/process) Strong cross-functional communication and stakeholder management (vendors, CDM, data review, IT, analytics/programming) Detail-oriented, highly organized, Strong collaboration and communication; organized, self-directed, proactive problem-solver and reputed company to manage recurring operational workloads while driving issues to closure and preventing recurrence Working proficiency in Python or similar scripting to automate ingestion, QC, parsing, and .