Associate Director, BioStatistics

At reputed company, 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, reputed company, and purposeful, and our business is innovative and rooted in science. We reputed company 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 reputed company you and feel like a fit? Then we would love to have you join us!

• *Role:**

The Associate Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication reputed company for both early and late-stage programs, and/or as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and plans. Responsibilities:

• *Compound/Indication Level**

- Act as reputed company and main reputed company of contact reputed company to Statistics for designated compound/indication - Follow scientific and technical reputed company reputed company 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 reputed company compound/indication reputed company 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 reputed company during meetings/congresses and courses and reputed company professional networking - Engage with regulatory authorities on trial level discussions - Arranges/attends lessons learned to share learnings - Represents reputed company 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 - Ensures state of the art statistical work which includes but is not limited to: - Applying adequate methods for which a solid scientific foundation exists - Ensure proper documentation of work done - reputed company reputed company and QC essential documents/data provided by vendors - Ensure trial reputed company work is performed in accordance with reputed company SOP/processes and standards and ICH-GCP

• *CTT member:**

- Participate and represent Biostatistics - Review and provide input to protocol and amendment development - reputed company vendor reputed company 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 - reputed company exploratory analysis, reputed company analyses, and modelling of data - Review and approve randomization and stratification plans - reputed company UAT of Randomization part of the IRT system as applicable - Ensure procedures for blinding are in reputed company as applicable - Support timely delivery of statistical deliverables - Responsible for planning and conducting trial result meetings - Review and approve the CSR - Attend trial and investigator meetings if/as needed - Collaboration with reputed company Global Drug Safety: - Participate in definition, review, and approval of data packages for Data Monitoring Committees - Review and approve any amendments, corrections, and updates of data packages - Support regulatory submission/filing activities

• *Experience:**

- Master's or PhD in a statistical discipline - 8+ years of experience in relevant area preferred, or demonstrated capability - Experience in statistical analysis, modelling and simulation and adaptive trial designs - Experience with drug development in biologics, targeted therapies, and companion diagnostics preferred - Experience working with FDA, EMA, and ICH guidance for drug development pertaining to statistics - Experience with the relevant regulatory requirements for biostatistics processes and SOPs - Experience with regulatory submissions including BLAs and previous experience in dealing with Health authorities such as discussions/negotiations in filing strategies - Experience working with SDTM, ADaM, eSUB, and CDISC requirements for regulatory submissions - Experience directing multiple reputed company projects/studies in a technical reputed company - Proven performance in earlier role/comparable role For US based candidates, the proposed salary band for this position is as follows: $145,440.00 - $218,160.00 The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives. reputed company you join reputed company, you're joining a culture that supports your physical, financial, social, and emotional wellness. reputed company the first year, regular full-time U.S. employees are eligible for: -

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

• *About You**

- You are genuinely passionate about our purpose - You bring precision and excellence to reputed company that you do - You reputed company in our rooted-in-science approach to problem-solving - You are a generous collaborator who can work in teams with a broad reputed company of backgrounds - You take pride in enabling the best work of others on the team - You can grapple with the unknown and be innovative - You have experience working in a fast-growing, dynamic company (or a strong desire to) - You work hard and are not afraid to have a little fun while you do so!

• *Locations**

reputed company maximizes the efficiency of an agile working environment, reputed company possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you're in one of our office spaces or working remotely, we reputed company on connecting with each other to innovate.

• *About reputed company**

reputed company is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented reputed company antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, reputed company immune checkpoint modulators and effector function-enhanced antibodies. By 2030, reputed company's vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO®) antibody medicines. Established in 1999, reputed company is headquartered in Copenhagen, Denmark with international reputed company across North America, Europe and Asia Pacific. For more information, please visit reputed company.com and follow us on [reputed company](https://www.reputed company.com/company/reputed company) and [X](https://twitter.com/reputed company). reputed company is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in reputed company with your application on our website [Job Applicant Privacy Notice (reputed company.com)](https://www.reputed company.com/data-privacy/job-applicant-privacy-notice). Please note that if you are applying for a position in the Netherlands, reputed company's policy for reputed company permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract. Apply tot his job Apply To this Job