Lead Statistical Programmer Consultant – CV/Renal Trials

ClinChoice; United States; On-site; USD 80,000 - 120,000; Full time

Benefits offered by this job

Professional development opportunities

Supportive work culture

Diversity and inclusivity initiatives

Job summary

ClinChoice is in search of a Principal Statistical Programmer/Analyst Consultant to contribute to cardiovascular and renal studies. The successful candidate will leverage strong SAS programming skills to support clinical projects, ensuring quality and timely deliverables.

This role requires a Bachelor's or Master's degree paired with several years of programming experience in the pharmaceutical sector. Join us at ClinChoice where we prioritize professional development and a supportive work culture.

Qualifications

• 5 years of clinical programming experience, preferably with CDISC.
• Strong communication skills and ability to work independently.
• Experience with regulatory submissions is a plus.

Responsibilities

• Develop and maintain SAS programs for clinical studies.
• Create datasets and reports according to study needs.
• Ensure high-quality standards for programming deliverables.
• Collaborate with teams to ensure project success.

Skills

SAS programming experience

Experience in cardiovascular studies

Knowledge of CDISC standards

Stakeholder management

Education

Bachelor's degree in computer science or related field

Master's degree preferred

Job description

ClinChoice is in search of a Principal Statistical Programmer/Analyst Consultant to contribute to cardiovascular and renal studies. The successful candidate will leverage strong SAS programming skills to support clinical projects, ensuring quality and timely deliverables.

This role requires a Bachelor's or Master's degree paired with several years of programming experience in the pharmaceutical sector. Join us at ClinChoice where we prioritize professional development and a supportive work culture.