Job Description
- Description:
- Supports the development of new therapies by ensuring integrity, consistency and adherence to standards of data
- Produces well-structured, high quality data summaries in tables, figures and listings for decision making.
- Leads programming activities while providing hands-on support.
- Reviews CRFs for adequacy and consistency
- Supports the establishment and maintenance of Genmab SDTM and ADaM database standards.
- Performs database standards consistency checks on databases delivered by the preferred DM & Statistics vendor.
- Produces other in-house checks of data consistencies.
- Performs sponsor oversight of programming activities.
- Maintains a good working relationship with stakeholders and colleagues.
- Requirements:
- Minimum BSc. or equivalent qualifications
- At least 2-5 years of experience within the pharmaceutical industry for Programming Manager, at least 6-8 years of experience for Senior Programming Manager
- Has experience working in a global context
- Proficient in both written and spoken English (Required)
- Proficient in writing SAS programs and macros to create analysis datasets and statistical summaries (tables, listings, and figures) (Preferred)
- Practical knowledge and experience using R to support clinical trial analyses.
- Benefits:
- 401(k) Plan: 100% match on the first 6% of contributions
- Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance
- Voluntary Plans: Critical illness, accident, and hospital indemnity insurance
- Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave
- Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support
- Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses
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