Principal Clinical Data Engineer

Data EngineerData EngineerFull TimeRemoteLeadTeam 10,001+Since 1983H1B SponsorCompany SiteLinkedIn

Location

South Africa

Posted

1 day ago

Salary

0

Seniority

Lead

Bachelor DegreeEnglishGoogle Cloud PlatformSQL

Job Description

Principal Clinical Data Engineer

Parexel

• Manage Projects & Technology • Lead and implement Data Receipt Agreements with vendors in collaboration with cross-functional teams • Program and establish import procedures for data ingestion using SAS or alternative technologies (e.g., Workbench) • Design and implement reconciliation checks to ensure accurate data transfer • Program offline listings and custom reports to provide valuable insights on external data • Aggregate data across all sources and manage data structures, missing values, and programming errors • Review data outputs and provide strategic insights to study teams and clients • Ensure first-time quality on all deliverables • Negotiate electronic data timelines and ensure adherence through active project management • Monitor project resourcing, identify scope changes, and resolve technical issues • Coordinate and lead programming teams to successful project completion within timelines and budget • Manage deployment of data management technology for offline listing creation • Act as SME and technology owner for data management offline listing platforms • Maintain comprehensive supporting documentation in accordance with SOPs, Guidelines, and Work Instructions • Ensure traceability and regulatory compliance across all study activities • Document deviations and communicate them to project teams • Support Initiatives & Continuous Improvement • Participate in creating standards through tools (SAS macros), libraries, and processes • Develop and implement project-specific tools and improvements • Lead or drive global initiatives related to processes and new technologies • Mentor staff and provide relevant training • Assist project teams in problem resolution and technical support • Maintain and expand regulatory knowledge within the clinical research industry • Serve as point of contact for clients and internal stakeholders on electronic data matters • Participate in bid defense meetings • Independently contribute ideas on technology and data engineering to support business development

Job Requirements

  • Bachelor's degree (or equivalent) in a relevant science discipline is preferred, or equivalent work experience
  • Advanced proficiency in at least one of the following: SQL, SAS, or R
  • Comprehensive knowledge of SOPs, Guidelines, Work Instructions, System Life Cycle methodologies, ICH-GCP, and applicable regulations (e.g., 21 CFR Part 11) with proven practical application
  • Strong experience working with at least two systems used to aggregate data in the clinical trial process (e.g., SAS, Workbench, Elluminate)
  • Written and oral fluency in English

Benefits

  • Health insurance
  • Professional development opportunities

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