Associate Director, Non-Clinical Safety

At Genmab we are dedicated to building extranotordinary 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

In this position you are part of the Global Non-Clinical Safety (NCS) team and report to the Head of the Non-Clinical Safety team. As a key member of international multidisciplinary project teams you work closely with NCS Leads and are the lead author of nonclinical toxicology documents.

This position can be based in our Princeton NJ or Copenhagen DK locations.

Responsibilities

• Represent NCS on global regulatory submissions project teams for Annual Reports Briefing Books Common Technical Documents Safety Update Reports Investigators Brochures INDs MAA and NDA/sNDAs

• Collaborate extensively with Global NCS team members to author coordinate monitor review and/or approve the nonclinical responses to Heathy Authorities for pending applications

• Expected to demonstrate an ability to work independently- producing high-quality documents with minimal supervision to meet timelines

• Manage and coordinate the completion of documents within established timelines and with high quality in terms of scientific content organization clarity accuracy format consistency and adherence to regulatory and internal guidelines styles and processes

• Escalate issues when necessary to maintain project timelines and performance standards

Requirements

• MS in toxicology pharmacology or related field required. PhD is preferred.

• At least 10 years of recent and relevant experience as a nonclinical writer of toxicology studies for biologics and/or pharmaceuticals.

• Extensive experience with Acumen DocuBridge or similar regulatory document submissions tools

• Strong project management organizational and communication skills (both written and verbal) to deliver clear updates on complex scientific information.

• Solid understanding of regulatory guidelines and document management standards.

• Speak and write in English fluently.

For US based candidates the proposed salary band for this position is as follows:

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.

When you join Genmab youre joining a culture that supports your physical financial social and emotional wellness. Within 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 all that you do

• You believe in our rooted-in-science approach to problem-solving

• You are a generous collaborator who can work in teams with a broad spectrum 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

Genmab maximizes the efficiency of an agile working environment when 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 youre in one of our office spaces or working remotely we thrive on connecting with each other to innovate.

About Genmab

Genmab 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 next-generation antibody technology platforms and harnessed translational quantitative and data sciences resulting in a proprietary pipeline including bispecific T-cell engagers antibody-drug conjugates next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030 Genmabs 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 Genmab is headquartered in Copenhagen Denmark with international presence across North America Europe and Asia Pacific. For more information please visit and follow us on LinkedIn and X.

Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice ().

Please note that if you are applying for a position in the Netherlands Genmabs policy for all 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.