Staff Engineer (Business Analyst - Clinical Trials)

REQUIREMENTS: 

• Experience : 6+ Years
• 6–8 years of experience as a Business Analyst or Data Analyst within the Life Sciences domain (mandatory).
• Experience with at least one Clinical Data Management or Analytics product implementation, such as:
  • EDC: Rave, Veeva, InForm
  • Non-EDC: ePRO, LAB systems
  • Other systems: Clinical Data Repository, Metadata Repository, statistical computing platforms (Sycamore, Nurocor, SAS), CTMS, eTMF, CDMS.
• Experience delivering or supporting end-to-end Clinical Data Repository implementation projects (preferred).
• Experience building or delivering GxP-compliant solutions for large enterprise programs (preferred).
• Exposure to clinical data standards such as CDISC SDTM and ADaM (preferred).
• Familiarity with programming languages like R, Python, and SAS (preferred).

RESPONSIBILITIES: 

• Drive requirements gathering, discussions, and workshops with internal and external stakeholders across global time zones.
• Coordinate planning and delivery activities for technology projects within the Life Sciences domain.
• Support implementation and configuration of Clinical Data Management and Analytics products (EDC, Non-EDC systems, CDR, MDR, CTMS, eTMF, CDMS, statistical computing tools).
• Work closely with cross-functional teams to ensure successful end-to-end Clinical Data Repository implementations, especially within Biometrics.
• Communicate project updates, issues, and analytical findings clearly to internal teams and client stakeholders.
• Contribute to the development of GxP-compliant technology solutions for large enterprise programs.
• Utilize knowledge of clinical data standards (CDISC including SDTM, ADaM) during project execution.
• Leverage programming skills (R, Python, SAS) to support data analysis, validation, or automation tasks where required.

Bachelor’s or master’s degree in computer science, Information Technology, or a related field.