Principal Clinical Rbqm Programmer

Biogen

Research Triangle Park, NC, United States
Base: $116,000.00-$155,000.00; bonus/equity: cash ...
Rbqm platform configuration and maintenance
Statistical programming with sas, r, python
Experience with cluepoints or equivalent rbqm tools
The Principal Clinical RBQM Programmer supports RBQM strategies by configuring platforms, interpreting outputs, and collaborating with cross-functional teams to ensure data integrity and compliance

Job Summary

  • The Principal Clinical RBQM Programmer supports RBQM strategies by configuring platforms, interpreting outputs, and collaborating with cross-functional teams to ensure data integrity and compliance.
  • Biogen offers a competitive compensation package including base salary, cash bonuses, equity incentives, and a comprehensive benefits program supporting employees’ physical, financial, emotional, and social well-being.
  • Biogen fosters a culture of inclusion and belonging, emphasizing diverse backgrounds and perspectives to drive innovation and impact in delivering life-changing medicines.

Matching Summary

The Principal Clinical RBQM Programmer supports RBQM strategies by configuring platforms, interpreting outputs, and collaborating with cross-functional teams to ensure data integrity and compliance.

Salary

Base: $116,000.00-$155,000.00; Bonus/Equity: Cash bonus and equity incentive opportunities; Benefits: Medical, Dental, Vision, Life insurance, wellness programs, paid time off, 401(k) with company match, tuition reimbursement

Skills & Requirements

Must-have

  • RBQM platform configuration and maintenance
  • Statistical programming with SAS, R, Python
  • Experience with CluePoints or equivalent RBQM tools
  • Clinical trial data standards and regulatory compliance
  • Data integration between RBQM and EDC systems
  • Dashboard and visualization development

Nice-to-have

  • Collaborative and proactive problem-solving mindset
  • Strong communication and presentation skills
  • Experience with clinical study analytics software
  • Familiarity with GCP and ICH guidelines
  • Process optimization and SOP development
  • Ability to manage multiple priorities under tight timelines

Key Requirements

  • 5+ years clinical data analytics or statistical programming
  • Bachelor’s degree in Computer Science, Statistics, Life Sciences or related field
  • Hands-on experience with CluePoints or equivalent RBQM tools
  • Proficiency in SQL, SAS, R, and Python
  • Strong understanding of clinical trial processes and CDISC standards
  • Excellent oral and written communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter