Sr Statistical Programmer

Ctifacts; Lisboa; Híbrido; EUR 45 000 - 65 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Hybrid work from home opportunities

Health benefits

Vacation package

Paid parental leave

Resumo da oferta

CTI Clinical Trial and Consulting Services is seeking an experienced Statistical Programmer in a hybrid role based in Portugal. You will lead programming tasks for studies, develop SDTM/ADaM specifications, and review TLFs and SAPs.

The position includes mentoring junior staff and collaborating with cross-functional teams. Ideal candidates have 5+ years of SAS programming experience in pharma/CRO settings, along with CDISC SDTM/ADaM mapping skills.

Qualificações

• 5+ years of statistical programming experience in pharmaceutical or CRO environment.
• Bachelor's degree in Statistics or Biostatistics.
• CDISC SDTM and ADaM dataset mapping experience.

Responsabilidades

• Assist with development and modification of SOPs and work instructions.
• Assist training and mentoring junior programmers.
• Develop macros to improve department efficiency and quality.
• Lead statistical programming on assigned studies and act as primary contact for project team members.
• Ensure programming tasks align with project timelines and communicate changes to management.
• Develop SDTM/ADaM specifications and TLF shells to support SAP analyses.
• Review SDTM-annotated CRFs and SAP reviews; provide feedback on TLFs.
• Perform data transfers between SAS and databases, ensuring data integrity.
• Maintain documentation in eTMF per project plans.

Conhecimentos

Statistical programming

SAS programming

CDISC SDTM/ADaM mapping

Mentoring/training

Formação académica

Bachelor's degree in Statistics or Biostatistics

Ferramentas

SAS

Descrição da oferta de emprego

• Assist with the development and modification of department SOPs and work instructions


• Assist with training new statistical programmer employees; mentor and assist junior level programmers


• Assist with the development of study bids and changes in scope for Statistical Programming tasks in response to prospective client's request for proposals (RFPs)


• Develop macros for department use that maximize efficiency and quality


• As the lead statistical programmer on the studies to which you are assigned, perform or oversee the following tasks:


• Act as primary statistical programming contact for internal and external project team members


• Work with the lead statistician to manage projects to ensure statistical programming tasks are performed within the entire project timeline. Keep Statistical Programming management aware of changes to project timelines.


• Proactively identify and communicate changes in scope to the clinical project manager and Statistical Programming management


• Provide SDTM naming conventions for database build specifications


• Develop, or oversee the work of others to develop, SDTM dataset specifications and assist with the development of ADaM dataset specifications and table, listing and figure (TLF) shells needed to perform the analysis defined in the Statistical Analysis Plan (SAP)


• Review/develop SDTM-annotated CRFs


• Perform the statistical programming to create SAS dataset deliverables, including SDTM and ADaM datasets, per dataset specifications


• Review Open CDISC findings and generate Reviewers Guide and Define.xml files


• Review the SAP and the TLF shells, and provide feedback to the statisticians


• Perform the statistical programming to create TLFs per mock TLF shells


• Perform data transfer activities between SAS and various databases and data file formats for internal team members (e.g., Clinical Data Management, Safety) and external clients (e.g., third party vendors, central labs), including file reconciliations


• Perform statistical programming to review data for protocol adherence, coding consistency and plausibility


• Carry out all activities according to CTI SOPs and project-specific conventions within the framework of Good Clinical Practice/ICH guidelines


• Rely on instructions and Biostatistics SOPs to ensure timely, standard, quality deliverables to customers


• Maintain accurate records of all work performed and ensure all relevant statistical programming documents are filed in the eTMF per the project-specific eTMF Plan


• Provide input to and participate in departmental meetings

What You'll Bring:

• At least 5 years of related statistical programming experience in either a pharmaceutical or CRO environment or other relatable statistical programming experience


• Bachelor's degree in Statistics or Biostatistics or demonstration of excellent technical ability in statistical programming procedures


• CDISC SDTM and ADaM dataset mapping experience

About CTI

CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com

Why CTI?

• Advance Your Career - We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.


• Join an Award-Winning and Valued Team - We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.


• Make a Lasting Impact - We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

Important Note

In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website ( www.ctifacts.com ) or from our verified LinkedIn page.

• We will never communicate with you via Microsoft Teams or text message


• We will never ask for your bank account information at any point during the recruitment process