Clinical Informatics Specialist

About Maxima Tek

We partner with top-tier companies to place exceptional recent graduates and experienced professionals (0-5 years) into high-impact, full-time Clinical Informatics Specialist and Statistical Reporting roles within the pharmaceutical and biotech sectors. We focus on connecting talent where it can truly thrive.

We are hiring for Entry-Level and Mid-Level full-time Clinical Informatics Specialist positions. This role involves using SAS programming to generate Tables, Listings, and Figures (TLFs) for clinical trial reports, performing data validation, and creating/maintaining CDISC standard datasets (SDTM/ADaM). You will collaborate closely with biostatisticians and data management teams.

• Education: Bachelor’s or Master’s degree in Biostatistics, Statistics, Computer Science, Public Health, or a related quantitative field (Required).
• Experience: 0-5 years of relevant experience in SAS programming or clinical data analysis.
• Technical
  
  Skills:
  
  
• Proficiency in SAS programming (Base SAS, SAS/STAT, SAS/MACRO) is mandatory.
• Understanding of the clinical trial process and regulatory guidelines (e.g., ICH).
• Familiarity with CDISC standards (SDTM and ADaM).
• Preferred
  
  Skills:
  
  Familiarity with clinical data management systems or other statistical software (R, Python).

• Targeted Placement: Direct marketing of your profile to hiring managers in Clinical Research and Pharma sectors.
• Expert Resume Rebuild: Personalized refinement to optimize your resume for Clinical SAS roles.
• Career Guidance: Dedicated support through the interview process.

Email your updated resume to:

• Entry level

• Full-time

• Consulting

• IT Services and IT Consulting

Cheyenne, WY $-$ 2 weeks ago

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