Programming Associate – Statistical Programming | Princeton, NJ
Job ID: R14389
Category: Clinical Data & Programming
Job Type: Full-Time / Entry-Level
Location: Princeton, New Jersey, United States
About Genmab
Genmab is a global biotechnology leader committed to improving patient outcomes through innovative antibody therapeutics. With over 25 years of experience, Genmab has developed cutting-edge platforms including bispecific T-cell engagers, antibody-drug conjugates, immune checkpoint modulators, and effector function-enhanced antibodies.
Headquartered in Copenhagen, Denmark, Genmab operates internationally across North America, Europe, and Asia-Pacific. By 2030, Genmab aims to transform cancer and serious disease treatment with its Knock-Your-Socks-Off (KYSO®) antibody medicines.
Learn more at www.genmab.com.
Role Overview
The Programming Associate in Statistical Programming is an entry-level position focused on developing expertise in clinical trial data programming. This role supports the creation of SDTM, ADaM datasets, and TLFs under supervision, contributing to high-quality clinical deliverables and regulatory-compliant outputs.
The ideal candidate is detail-oriented, collaborative, and eager to develop skills in clinical data standards, statistical programming, and regulatory guidelines.
Key Responsibilities
Execute programming tasks under close supervision, including SDTM, ADaM, and TLF development.
Conduct quality control (QC) and support sponsor oversight activities.
Develop proficiency in company-standard coding practices and tools.
Build technical skills in data manipulation, visualization, and reporting.
Participate in internal programming meetings and training sessions.
Maintain knowledge of study-level documentation and contribute to inspection readiness.
Adhere to version-control discipline, good programming practices, and company standards.
Continuously update knowledge of ICH guidelines, regulatory requirements, CDISC fundamentals, and therapeutic areas.
Qualifications
Education: Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, or related fields.
Experience: Entry-level; 0 years relevant experience required.
Basic understanding of programming concepts; exposure to SAS, R, or other statistical software preferred.
Interest in clinical data standards (e.g., CDISC SDTM, ADaM) and regulatory compliance.
Strong attention to detail, organizational skills, and ability to work in a collaborative, fast-paced environment.
Compensation and Benefits (US-Based Candidates)
Salary Range: $80,800 – $121,200 annually (based on experience, qualifications, and location).
Eligibility for discretionary bonuses and long-term incentives.
Comprehensive medical, dental, and vision coverage.
401(k) plan with company match.
Paid vacation, sick leave, holidays, and 12 weeks of discretionary parental leave.
Access to wellness, financial, and lifestyle support programs.
Commuter benefits, tuition reimbursement, and Lifestyle Spending Account for wellness and personal expenses.
About You
Passionate about clinical data programming and advancing patient-centered research.
Collaborative and proactive, with strong attention to detail.
Eager to learn, innovate, and grow in a dynamic, fast-paced environment.
Committed to ethical practices and regulatory compliance.
Open to mentorship and continuous professional development.
Gujarat :
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