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Mid-level metro role with 3+ years requirement and a well-known CRO increases applicant competition.
Clinical Rave and SAS programming skills are highly specific to pharma/CRO environments, limiting portability.
Mandates Rave EDC and CRF/edit-check programming plus GCP, creating strict mandatory filters.
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Design, write, validate, and maintain clinical programming software using tools like Medidata RAVE, Oracle RDC, and SAS according to specifications.
Lead and coordinate clinical programming activities across multiple concurrent studies, managing resources and timelines effectively.
Develop and review study-specific documentation including CRF annotations, database configurations, edit checks, and reports; support audits and ensure quality deliverables.
Minimum 3 years of relevant experience specifically in Medidata RAVE EDC build including CRF or screen build and edit checks programming.
Bachelor’s degree preferred or equivalent combination of education and experience.
Good knowledge of Good Clinical Practices (GCP).
Experience with programming languages such as PL/SQL, SAS, C#, or VB preferred but not mandatory.
Proven capability to manage and lead clinical programming across multiple studies in a matrix-structured environment.
Strong technical expertise in clinical data management and programming tools relevant to RAVE EDC environments.
Experienced in interacting with project management and clients, able to communicate project status, risks, and resource needs clearly and proactively.