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Clinical Data Analyst

Redwood City, CA 94063

Posted: 03/08/2024 Employment Type: Contract Job Category: Data Sciences Job Number: 595579 Is job remote?: No Country: United States

Job Description

Contract Clinical Data Analysis – Clinical Data Sciences
 
  • Collaborate with data managers, statistical programmers, biostatistics, clinical operations, and external vendors to review, sign off on the data transfer specifications, and transfer data from external sources, ensuring data is received and validated for data integrity.
  • Collaborate in the development of programming specifications and the creation of program-specific validation plans using established validation practices and processes.
  • Provide robust technical SAS programming expertise to support data management, including the development, validation, implementation, and maintenance of data review listings, metrics, dashboards, and reconciliation reports for all studies.
  • Work experience in using CRF-Annotation, FDA regulations such as CDISC, 21 CFR Part 11, ICH, GCP guidelines, and other regulatory submissions to the NDA.
  • Participate in the development and implementation of SAS programming standards, SOPs, and work instructions, including program validation and documentation.
  • Work with data managers and generate outputs to support data cleaning, enhance data integrity, and ensure timely, targeted, and accurate deliverables.
  • Ensure quality and timely delivery of clinical trial data in preparation for data review and statistical review.
  • Address data issues identified by cross-functional team members.
  • Ensure accuracy of clinical trial results for internal and external audiences (e.g., regulatory authorities).
  • Contribute to the development of SAS macro programs and participate in modifying existing SAS macro programs to improve efficiency throughout the project life cycle.
Specific required experience, skills, and education:
  • MS, BS/BA degree or other suitable qualification with relevance to the field.
  • Custom reporting using Business Objects, SAS, Python, Crystal Reports, and understanding of Medidata Rave Study Build is required.
  • Demonstrated ability to multi-task, prioritize options, anticipate challenges, and execute on goals as a member of an interdisciplinary team is extremely important.
  • Should have real-time 6+ years of work experience in Phases I, II, and III oncology clinical trial studies.
  • Quick learner, self-starter, effective troubleshooter, and good at resolving data issues, committed to continuous learning and improvement, and should be a team player.
  • Effective written and oral communication skills required.
  • Possessing SAS certification, work experience in Spotfire or Tableau or Power BI and windows batch script is preferred.
Our client currently requires that all personnel and visitors to its offices be fully vaccinated against COVID-19. This role will require that the employee meet with company employees and work from the company’s offices. Given that these essential functions of the role must be performed on-site, this position requires full COVID-19 vaccination, subject to applicable law.
 
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About Redwood City, CA

Ready to embark on an exciting career opportunity in the vibrant area around Redwood City, California? Nestled in the heart of Silicon Valley, this thriving region offers a perfect blend of innovation, growth, and charm. From the bustling tech scene to the serene beauty of Redwood City's parks, like Edgewood Park and Pulgas Ridge Preserve, there's something here for everyone. Immerse yourself in the local culture by visiting the Fox Theatre or exploring art galleries like The Art Center and Redwood City Art Kiosk. With a bustling food scene offering everything from trendy cafes to authentic Mexican cuisine, it's no wonder that Redwood City is a top choice for job seekers looking to thrive in a dynamic environment. Browse our job listings today and take the next step towards a fulfilling career in this captivating locale!

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