Senior Manager, Biostatistics

Genmab

106d • $122,000 - $183,000

About The Position

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so. Does this inspire you and feel like a fit? Then we would love to have you join us! The Role The Senior Manager, Biostatistics acts as a biostatistician supporting the clinical development of compounds as compound lead, primarily up until proof of concept, and/or as trial responsible statistician.

Requirements

• MS / PhD or equivalent in a statistical discipline.
• 5+ years of experience in relevant area preferred or demonstrated capability.
• Experience in statistical analysis, modelling and simulation and adaptive trial designs.
• Experience in working with clinical trials.
• Preferred experience with oncology clinical trials.
• Proficient programming skills in statistical software’s, such as SAS.
• Excellent oral and written communication skills.
• Ability to work independently as well as in teams.
• Confident, self-reliant, and a quick learner.
• Proactive and open-minded.
• Ability to prioritize and work in a fast-paced and changing environment.
• Result and goal-oriented and committed to contributing to the overall success of Genmab.

Responsibilities

• Act as lead and main point of contact related to Statistics for designated compound/indication.
• Follow scientific and technical progress within the field of biostatistics in drug development and advise of new methodologies that may support innovation and improve efficiencies.
• Engage with regulatory authorities on compound/indication level discussions.
• Act as a role model.
• Ensure consistency of statistical methods and data handling across trials.
• Ensure all compound/indication related work and information is shared between biostatisticians involved in the compound and with the vendor.
• Support compound responsible programmer in developing an integrated database specification.
• Responsible for giving statistical input to overall strategy and the synopsis development in the CDT.
• Provide scientific advice to the CDT including design of trials, analyses and analyses requiring advanced statistical methodologies/techniques.
• Represent the CDT/the company at regulatory meetings, during Key Opinion Leaders meetings, network and/or Partner meetings, as applicable.
• Drive design and synopsis development together with relevant stakeholders.
• Ensure transparent communication to relevant stakeholders from the CDT.
• Ensure availability of integrated database(s), as needed, and planning and conduct of integrated analysis to support development decisions, submissions, and marketing needs.
• Support development and communication in relation to communication strategy and/or scientific input to presentations, posters, and articles.
• Represent Genmab during meetings/congresses and courses and perform professional networking.
• Engage with regulatory authorities on trial level discussions.
• Arrange/attend lessons learned to share learnings.
• Ensure biostatistician review of partner synopsis, protocols, statistical analysis plans, results meetings presentations and clinical trial reports.
• Coordinate data transfers from/to business partners in collaboration with the programmer and the data manager, as applicable.
• Participate and represent Biostatistics in CTT meetings.
• Review and provide input to protocol and amendment development.
• Perform vendor oversight according to applicable SOPs.
• Give input to eCRF setup, edit checks, validation plan, protocol deviations classifications, DSUR, IB updates, tables, figures, and listings etc.
• Review assay validation reports, as applicable.
• Perform exploratory analysis, ad hoc analyses, and modelling of data.
• Review and approve randomization and stratification plans.
• Perform UAT of Randomization part of the IRT system as applicable.
• Ensure procedures for blinding are in place as applicable.
• Support timely delivery of statistical deliverables.
• Responsible for planning and conducting trial result meetings.
• Review and approve the CSR.
• Attend operational and steering committee meetings, as applicable.
• Support regulatory submission/filing activities.

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.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Master's degree
• Number of Employees: 1,001-5,000 employees