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Summary
About the Role
About You
- Bachelor's degree in Mathematics, Statistics, Biostatistics, Epidemiology, or related scientific field.
- 5+ years of experience with statistical programming in the CRO, medical device, or pharmaceutical industry.
- Expertise in R programming and SAS Base, with knowledge of SAS graph and SAS Macros.
- Strong knowledge of data standards for clinical research including CDISC SDTM and ADaM.
- Experience and familiarity with medical devices.
- Understanding of quality control related to regulatory documentation requirements.
- Experience with adaptive trials and Bayesian analysis techniques.
Benefits
- Competitive salary and benefits package.
- Opportunities for professional development and growth.
- Collaborative work environment with a focus on innovation.
MCRA, an IQVIA business, is a leading full-service medical device, diagnostics, and biologics CRO and consulting advisory firm helping global healthcare companies maximize the value of their innovations. Using an integrated approach informed by the entirety of the commercialization process, we propel healthcare innovations in all stages of development through the product pathway. MCRA offers Regulatory, Clinical Research, Reimbursement, Healthcare Compliance, Quality Assurance, Due Diligence, AI & Imaging, Digital Health, Talent Solutions, and Cybersecurity services. Our exceptional team includes 25+ former FDA officials, payer medical directors, industry veterans, and partners from the world’s most respected medical institutions. We have extensive expertise in the therapeutic areas of orthopedics, spine, biologics, cardiovascular, diagnostic imaging, wound care, artificial intelligence, dental, anesthesia, general surgery, digital health, neurology, robotics, oncology, general and plastic surgery, urology, in vitro diagnostic (IVD) devices, regenerative medicine and more. At MCRA, we work at the speed of science, and our world-class expertise unlocks multiple barriers to success. To learn more, visit mcra.com.