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Senior Programming Associate / Programming Manager

2+ years
$76.500,00-$127.500,00
10 Sept. 27, 2024
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Genmab: Building Extraordinary Futures Together

At Genmab, we are dedicated to transforming the future of cancer treatment and serious diseases by developing innovative antibody products and pioneering therapies. Our team is composed of caring, candid, and impact-driven individuals who thrive in a culture of authenticity and uniqueness. We believe that our diverse perspectives and relentless determination are crucial to fulfilling our mission of improving patients' lives.


The Role & Department

Position: Senior Programming Associate / Programming Manager

In this role, you will play a vital part in the development of new therapies by ensuring the integrity, consistency, and adherence to data standards. You will produce high-quality data summaries in tables, figures, and listings that support critical decision-making.

You will work closely with the Lead Programmer and collaborate with teams in Data Management, Statistics, Drug Safety, Medical Affairs, Clinical Pharmacology, and Biomarker functions, developing and writing SAS or other programming languages.


Key Responsibilities

  • Data Review and Standards: Assess CRFs for adequacy and consistency; establish and maintain Genmab’s SDTM and ADaM database standards; perform consistency checks on databases from vendors.

  • Analysis and Deliverables: Produce analysis datasets, tables, figures, and listings for various regulatory submissions and internal analyses, ensuring quality control before formal release.

  • Programming Oversight: Aid in sponsor oversight of programming activities with vendors and perform quality checks on SAS code written by colleagues.

  • Regulatory Compliance: Ensure programming components comply with electronic submission standards and regulatory guidelines.

  • Process Improvement: Contribute to developing standard processes and templates, support resource planning, and foster knowledge sharing and collaboration across teams.

  • Stakeholder Engagement: Maintain good relationships with stakeholders, participate in meetings, and represent programming in team discussions.


Requirements

  • Educational Background: Bachelor’s degree in a relevant field or equivalent qualifications.

  • Experience: Minimum of 2 years in the pharmaceutical industry as a Programmer, with proficiency in SAS and familiarity with programming languages like R and Python.

  • Language Skills: Proficient in written and spoken English.


Competencies and Skills

  • Strong SAS programming skills.
  • Analytical and problem-solving capabilities.
  • Knowledge of CDISC, SDTM, and ADaM data models.
  • Ability to write efficient and well-documented programs.
  • Organized, thorough, and proactive in task management.
  • Excellent communication and planning skills.
  • Ability to manage multiple tasks without compromising quality.

Work Environment

This role is based in Genmab's offices in Princeton, NJ; Copenhagen, Denmark; or Utrecht, the Netherlands, and supports a hybrid work model. Remote work may be considered for candidates outside local commuting distances, with preference for those in Eastern or Central Time Zones (US) or European time zones.


Compensation

For US-based candidates, the salary range for this position is $76,500 to $127,500, with the final offer considering your skills, qualifications, experience, and location. Additional forms of compensation, such as bonuses, may be available for certain roles.


About You

You are passionate about our mission to transform patients' lives through innovative cancer treatments. You bring rigor and excellence to your work and thrive in collaborative environments. You are committed to tackling challenges with creativity and determination and have experience in dynamic, fast-growing companies.


About Genmab

Genmab is a leading biotechnology company focused on improving patient lives through innovative antibody therapeutics. With over 20 years of experience, we have developed next-generation antibody technology platforms and maintain a robust pipeline of bispecific T-cell engagers, immune checkpoint modulators, and more. We are committed to fostering workplace diversity and inclusivity, ensuring that all team members are respected and valued.


Apply by February 12, 2024, to be part of our mission to create Knock-Your-Socks-Off (KYSO™) antibody medicines that change lives.

For more information about our commitment to diversity, equity, and inclusion, and to view our privacy policy regarding personal data protection, please visit our website.