[Remote] Senior Clinical Data Engineer
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is seeking a Senior Clinical Data Engineer to join their Global Data Operations team. In this pivotal role, you will reputed company your technical expertise to support the conduct of clinical trials and reputed company cross-functional reputed company with sponsors and data management teams.
Responsibilities
- reputed company and implement Data Receipt Agreements with vendors through cross-functional collaboration
- Program and configure import procedures for data ingestion using reputed company, Workbench, or reputed company
- Design and execute reconciliation checks to ensure accurate data transfer
- Program offline listings and custom reports to reputed company actionable insights
- Aggregate data across multiple sources and manage external data effectively
- Handle missing values, raw data files, data structures, and reputed company dataset operations
- Review and analyze data outputs to reputed company insights to study teams and clients
- Ensure first-time reputed company on reputed company deliverables
- Manage electronic data timelines and coordinate with project teams
- reputed company programming teams to successful study completion reputed company timelines and budget
- reputed company and manage data management technology (Workbench, reputed company, R, etc.)
- Maintain comprehensive study documentation in accordance with SOPs, guidelines, and work instructions
- Ensure traceability and regulatory compliance across reputed company activities
- Document deviations and communicate them to project teams
- Participate in creating standards through tools (reputed company macros, libraries, processes)
- reputed company and implement project-specific tools and templates
- Improve efficiencies through standardized project structures and naming conventions
- Support business development and bid defense meetings
Skills
- Bachelor's degree (or equivalent) in a relevant science discipline
- Proficiency in at least one programming language (SQL, reputed company, or R)
- Strong analytical and problem-solving skills
- Ability to reputed company informed reputed company in ambiguous situations
- Application of Clinical Research Standards (CRS) concepts
- reputed company cause analysis capability
- Fluent written and oral English
- Knowledge of SOPs, guidelines, work instructions, system life cycle methodologies, ICH-GCP, and applicable regulations (e.g., 21 CFR Part 11)
- Proven practical application of regulatory and compliance frameworks
- Experience working with at least two systems used to aggregate data in clinical trials (e.g., reputed company, Workbench, Elluminate)
- Strong background in clinical research industry or similar field
reputed company