The Senior Clinical Programming role is fully remote and begins on an initial 12-month contract with opportunity for extension. This clinical-stage biotechnology company focuses within precision medicines for kidney diseases.
Responsibilities:
-Produce timely, high quality, and reliable clinical trial data, listings, reports, and trackers for data cleaning, data review, and study status tracking
-Provide input to the clinical data reporting requirement to ensure high quality deliverables
-Perform ingestion activities of multiple external data (Safety, ePRO, IRT, PK, etc)
-Collaborate with internal stakeholders and cross functional team members within Biometrics, Clinical Operations, and Clinical Development
Requirements:
-5+ years experience supporting clinical programming and techinical data management activities fo rall phases of clinical trials
-Solid knowledge of pharmaceutical and regulatory requirements
-Excellent SAS programming skills, with a thorough understanding of clinical data structures, Proc SQL, SAS macro
-Experience with EDC applications, preferably Rave EDC or Veeva CDMS
-Experience with varied business intelligence and analytic tools, Looker, Qlik Sense, Spotfire, Tableau, Power BI, and/or SAP BusinessObjects
-Excellent interpersonal skills and demonstrated ability to establish and maintain professional and productive cross-functional working relationships
