Senior Clinical Programmer

Job Summary

To support clinical research initiatives, the remote Senior Clinical Programmer will lead the development of data acquisition standards, provide expertise in EDC and CDISC practices, and oversee database design and programming while collaborating with cross-functional teams.

Key responsibilities

• Develop and maintain global standards for data collection, acquisition, archival, and submission in compliance with CDISC and regulatory guidance
• Provide leadership for database design, programming, and training activities while mentoring team members
• Define regulatory-compliant data exchange standards with external partners and oversee vendor activities across multiple trials

Required qualifications

• Minimum of 8 years of relevant experience in the pharmaceutical or biotechnology industry
• Demonstrated experience developing clinical databases such as Medrio, Medidata Rave, or Oracle InForm
• Proficiency in programming and reporting tools including J-Review, Spotfire, SAS, Java, and C
• Bachelor's degree in Computer Science, Life Sciences, or a related field, or equivalent experience required; advanced degree is a plus
• Strong understanding of ICH, GCDMP, CDISC, and GCP guidelines