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Senior Manager, Biostatistics
Job in
Princeton, Mercer County, New Jersey, 08543, USA
Listed on 2025-12-27
Listing for:
The Antibody Society
Full Time
position Listed on 2025-12-27
Job specializations:
-
IT/Tech
Data Scientist
Job Description & How to Apply Below
At Genmab, we build extraordinary futures through the development of antibody products and groundbreaking KYSO® antibody medicines that change lives and advance cancer treatment.
The RoleThe 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.
ResponsibilitiesCompound/Indication Level
- 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
- Acts as a role model
- Ensures consistency of statistical methods and data handling across trials
- Ensures all compound/indication related work and information is shared between biostatisticians involved in the compound and with the vendor
- Supports compound responsible programmer in developing an integrated database specification
CDT member
- 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
Trial Level
- Represent Genmab during meetings/congresses and courses and perform professional networking
- Engage with regulatory authorities on trial level discussions
- Arranges/attends lessons learned to share learnings
- Represents Genmab during Key Opinion Leaders meetings
- 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
CTT member
- Participate and represent Biostatistics
- 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
- 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
For US based candidates, the proposed salary band for this position is: $ – $. The actual salary offer will…
Position Requirements
10+ Years
work experience
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