Clinical Data Programming Lead

As Clinical Data Programming Lead you are responsible for specifying, developing, validating and executing programs and generation of clinical data work.

Home or office based in USA, Mexico or Europe

• Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets.
• Build SDTM data set specifications per specified study requirements.
• Program data sets per specification.
• Validate data sets per the formal, documented CC process.
• Build data programming specifications per specified study requirements.
• Program clinical data programs per specification.
• Validate clinical data programs per the formal, documented CC process.
• Craft and maintain study documentation as required, in accordance with ICON Standard Operating Procedures.
• Execute programs and generate clinical data outputs to according to study/client requirements.
• Review and quality assure CRF annotations produced by other programmers.
• Review and quality assure supporting documentation produced by other programmers.
• Participate in testing of clinical data system upgrades and documenting of test scripts when required.
• Adhere to Data Management department quality control procedures.
• Liaise with other ICON functions & sponsors as needed.
• To undertake other reasonably related duties as may be assigned from time to time.
• Contribute to department process improvements, SOPs and WPs
• Lead programming and validation activities across a single project, ensuring that timelines are met and deliverables are of sufficient quality.

Requirements:

• Proven SQL & SAS programming experience with clinical data management experience.
• Successfully handle multiple tasks and timelines.
• Demonstrated ability to perform work you're leading individually.
• Demonstrated ability to liaise expertly with team members.
• Team player with strong verbal and written communication skills
• Proven ability to learn new technologies, applications and techniques o
• Advanced knowledge of the clinical data programming development life cycle, Advanced knowledge of clinical data programming concepts.
• Associate's degree in information systems, science or related discipline or meaningful experience required