Senior Manager, Clinical Trial Disclosure Specialist

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

Genmab is committed to transparency of clinical trial research. We recognize the scientific and ethical value of sharing clinical trial information in a non-biased and timely manner to benefitpatients and other external stakeholders. The Clinical Trial Disclosure & Transparency (CTD&T) team resides within Development Operations which hosts key functions for ensuring successful conduct and reporting of clinical trials.

We are now looking for a new Senior Manager to join our CTD&T team. The role offers a meaningful blend of operational and strategic tasks in a collaborative environment where quality shared purpose and cross-functional support are central to how we work.

In the role as Senior Manager of CTD&T you will be executing against the global and national disclosure regulations and requirements across the entire Genmab portfolio. This role engages with internal and external stakeholders to ensure consistent and responsible disclosure and transparency practices. The position requires strong expertise in disclosure requirements and regulatory processes coupled with strong organizational and communication skills while maintaining a commitment to quality integrity and advancing Genmabs mission.

Responsibilities

• Manage track and maintain overall responsibility for the disclosure of clinical trial protocols and results on EU CTIS and other applicable registries/platforms.

• Support and provide guidance on redaction activities.

• Ensure development of plain language results summaries.

• Stay updated on industry guidelines to ensure compliance.

• Support in updating SOPs contribute to process improvements and maintain adherence to established standards.

• Oversee vendor performance related to transparency deliverables.

• Liaise with clinical CROs to ensure consistent messaging across study registries.

• Deliver training on Genmabs disclosure processes to internal staff and provide guidance to CROs and vendors as needed.

• Ensure internal teams are informed of updated or new requirements and laws.

• Ensure management of unsolicited requests received via the mailbox.

Requirements

• 5 years of clinical trial disclosure experience including a Bachelors or Masters degree with relevant specialization.

• Strong knowledge of disclosure requirements technology and platforms.

• Proven ability to lead projects and facilitate cross-functional collaboration.

• Excellent written and verbal communication.

• Previous experience as a Medical Writer is advantageous given the close alignment between the CTD&T and Medical Writing teams.

Moreover you meet the following personal requirements:

• Engaged colleague with a positive and collaborative mindset.

• Strong organizational skills; able to manage conflicting priorities.

• High level of integrity accuracy and attention to detail.

• Quality mindset with the ability to prioritize in a fast-paced and evolving environment.

• Result- and goal-oriented committed to contributing to Genmabs success.

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.