One million success stories. Start yours today.

Senior Manager, Clinical Programming

Date Posted: May 29, 2026
Yearly: USD - USD
Job is expired

Job Detail

  • location_on
    Location Plainsboro, New Jersey, United States of America
  • desktop_windows
    Job Type: Permanent
  • schedule
    Shift:
  • analytics
    Career Level:
  • group
    Positions:
  • calendar_view_day
    Experience:
  • male
    Gender: No Preference
  • school
    Degree:
  • calendar_month
    Apply Before: Jun 29, 2026
Email to Friend Add to Favourite Report Abuse

Job Description

Overview

Genmab is seeking a Senior Manager of Clinical Programming to oversee the establishment and governance of Study Data Tabulation Model (SDTM) standards. This role involves ensuring data quality and consistency across programs and systems while collaborating with internal and external stakeholders to support clinical trials.

Key responsibilities

  • Develop and implement SDTM standards supporting scientific and compliance needs.
  • Ensure alignment of SDTM standards with data collection and relevant company tools.
  • Serve as a subject matter expert on standards development, industry standards, and regulatory requirements.
  • Ensure compliance of SDTM datasets with CDISC and regulatory submission requirements.
  • Support the knowledge development of others in data standards and reporting.
  • Create quality control processes and documentation for standards management.
  • Define standards specifications and collaborate with implementation teams.
  • Facilitate continuous process improvement and high customer service levels.
  • Support technology-enabled processes and tools for clinical trial standards.
  • Liaise between Clinical Programming and External Data Management for SDTM deliverables.

Required skills

  • Bachelor's degree in Statistics, Computer Science, or Life Sciences; Master's preferred.
  • 6-8 years of relevant experience in pharmaceutical, biotech, or CRO environments.
  • Proficient in SAS programming with 6-8 years of experience.
  • Practical knowledge of R for clinical trials preferred.
  • Knowledge of clinical research, metadata management, and regulatory requirements.
  • Experience managing multiple tasks and cross-functional projects.
  • Strong verbal and written communication skills.
  • Experience in clinical data management and standards management preferred.

What the company offers

  • 401(k) Plan: 100% match on the first 6% of contributions.
  • Health benefits including medical, dental, and vision insurance.
  • Paid vacation, sick leave, and holidays.
  • 12 weeks of discretionary paid parental leave.
  • Access to backup care and family support programs.
  • Commuter benefits and tuition reimbursement.

Skills Required

Company Overview

Genmab
Los Angeles, Baja California, United States of America
8 Current Jobs Openings

Genmab is dedicated to building extraordinary futures through innovative antibody products and groundbreaking medicines aimed at changing lives and the future of cancer treatment. The company values unique contributions and strives to maintain a glob... Read More

Google Map

Related Jobs