This is a fully remote position, open to applicants in Ukraine, +4 more countries.

📋 Description

• Oversee or assist with programming tasks for intricate phase I–III clinical trials

• Strategize, implement, and manage study programming initiatives, including resource forecasting, budget oversight, timelines, quality assurance, and collaboration with cross-functional teams/clients

• Create and maintain SAS programs for generating SDTM and ADaM datasets along with TFLs

• Conduct quality checks on SDTM, ADaM datasets, and TFLs

• Generate Define XML/PDFs, Analysis Results Metadata (ARM), annotated eCRFs, and Review Guides

• Collaborate with senior programming support to develop SDTM and ADaM dataset specifications

• Evaluate SAPs and TFL templates from a programming standpoint

• Address QA and client audits with guidance from senior programming support

• Undertake additional assigned responsibilities

⛳️ Requirements

• A minimum of a Bachelor’s degree, ideally in mathematics, statistics, computing, life sciences, health sciences, or related fields

• Generally, 1–2 years of SAS® programming experience within the CRO or Pharmaceutical sector, or a comparable blend of education and experience

• Familiarity with CDISC standards

• Proficient business English, both spoken and written

🏝️ Benefits

• Fully remote work option

• Option to work from a local office in your home country

• Chance to lead studies across multiple phases of the clinical development plan

• Assistance for submissions, regulatory inquiries, publications, and ad hoc/post hoc requests