Clinical Data Management

VeracyteSan Diego, CA
84d$1 - $1Remote

About The Position

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way - it's about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.

Requirements

  • Bachelor's degree in Computer Science, Life Sciences, or related field
  • 4+ years hands-on experience in IVD, Medical Device, or Pharmaceutical clinical data management
  • Knowledge of GCP and GCDMP
  • Proficiency in programming languages (R, SAS)
  • Proficiency in database management (SQL, PL/SQL)
  • Experience with EDC systems and clinical data management platforms (e.g. Medidata, Medrio)
  • Experience with CTMS and eTMF platforms with strong preference for experience with Veeva Vault
  • Experience with sample management platforms (e.g. LabVantage)
  • Proficiency in Microsoft Office Suite

Nice To Haves

  • Experience with CDISC/CDASH/SDTM/ADAM standards
  • Familiarity with FDA guidelines and regulations
  • Experience with database validation and quality control processes
  • Experience with clinical trials
  • Experience with Medidata
  • Experience with Veeva Vault
  • Experience with LabVantage
  • Knowledge of clinical trial data workflows

Responsibilities

  • Support end-to-end clinical data management operations, from protocol design to database closure
  • Support the implementation of comprehensive data management plans, validation specifications, and quality control procedures
  • Participate in the design and validation of eCRF systems and edit checks aligned with protocol requirements
  • Support database development, validation programming, and query management
  • Collaborate with Clinical Affairs, Data Analysis, and IT teams to establish data collection methods and quality standards
  • Generate key metrics reports and data analytics for clinical studies.

Benefits

  • Competitive compensation and benefits
  • Discretionary bonuses/incentives
  • Restricted stock units
  • Career opportunities in a growing company
  • Inclusive workforce fostering diverse backgrounds

Stand Out From the Crowd

Upload your resume and get instant feedback on how well it matches this job.

Upload and Match Resume

What This Job Offers

Career Level

Mid Level

Industry

Ambulatory Health Care Services

Education Level

Bachelor's degree

© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service