Senior Statistical Programmer

Planet Pharma; Town of Poland (NY); On-site; USD 48,000 - 81,000; Full time

Job summary

Planet Pharma is seeking a Senior Statistical Programmer to lead programming activities for global clinical trials and support regulatory submissions. The role focuses on delivering high-quality SDTM and ADaM outputs, developing SAS macros, and guiding cross-functional teams within a Biometrics Center of Excellence.

Ideal candidates will have 4+ years of clinical trial statistical programming with strong SAS experience, CDISC SDTM/ADaM expertise, and excellent analytical and communication

Qualifications

• Master's or PhD in Statistics, Biostatistics, Epidemiology, Computer Science, or related field with 4+ years of clinical trial statistical programming experience.
• Bachelor's degree with 6+ years of clinical trial statistical programming experience.
• Strong SAS programming experience in a clinical research environment.
• Hands-on CDISC SDTM/ADaM standards and regulatory submission deliverables.

Responsibilities

• Lead statistical programming activities and ensure timely, high-quality delivery of clinical trial outputs.
• Develop, program, and validate SDTM and ADaM datasets following CDISC standards.
• Perform quality control reviews of datasets, TLGs, and define.xml files.
• Support regulatory submission activities and ensure compliance with programming standards and SOPs.
• Develop and maintain SAS macros, utilities, and programming processes to improve efficiency.
• Provide technical guidance and contribute to continuous improvement initiatives.

Skills

SAS programming

CDISC SDTM/ADaM

Statistical programming

Analytical skills

Communication skills

Education

Master's or PhD in Statistics/Biostatistics/Computer Science

Bachelor's degree in a related field

Tools

SAS

SAS macros

Job description

Join a growing global Biometrics team at an exciting stage of expansion. Our client is building a dedicated Biometrics Center of Excellence in Poland and looking for talented Statistical Programmers who are passionate about data, innovation, and making an impact in clinical research.

As a Senior Statistical Programmer, you will play a key role in delivering high-quality statistical programming solutions across global clinical trials, supporting regulatory submissions, and collaborating with cross-functional teams worldwide.

Key Responsibilities

• Lead statistical programming activities and ensure timely, high-quality delivery of clinical trial outputs.
• Develop, program, and validate SDTM and ADaM datasets following CDISC standards.
• Perform quality control reviews of datasets, TLGs, and define.xml files.
• Support regulatory submission activities and ensure compliance with programming standards and SOPs.
• Develop and maintain SAS macros, utilities, and programming processes to improve efficiency.
• Provide technical guidance and contribute to continuous improvement initiatives.

Qualifications

• Master\'s or PhD degree in Statistics, Biostatistics, Epidemiology, Computer Science, or a related field with 4+ years of clinical trial statistical programming experience,

OR

• Bachelor\'s degree in a related field with 6+ years of clinical trial statistical programming experience.
• Strong SAS programming experience in a clinical research environment.
• Hands-on experience with CDISC SDTM/ADaM standards and regulatory submission deliverables.
• Strong analytical, problem-solving, and communication skills.

Why Join?

Be part of a newly established Biometrics team where you can make an immediate impact, collaborate with global experts, and help shape the future of clinical research. This is an opportunity to grow your career while contributing to meaningful scientific advancements.

About Planet Pharma:

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

www.planet-pharma.com