Associate Director, Trial Delivery Team Lead

Genmab; Princeton (NJ); On-site; USD 159,000 - 238,000; Full time

Benefits offered by this job

401(k) Plan: 100% match on the first 6

Health Benefits: Two medical plan with

Voluntary Plans: Critical illness, etc

Time Off: Paid vacation, sick leave, &

Support Resources: backup care & well‑

Additional Perks: Lifestyle Spending

Job summary

Genmab seeks an Associate Director, Trial Delivery Team Lead to oversee CTMs and CTAs, ensuring high-quality clinical trial execution. You will mentor teams, optimize resource use, and align with regulatory standards.

You may assume GTL responsibilities and drive process improvements within the Development Operations organization, collaborating with senior leadership to implement best practices.

Qualifications

• 12+ years of experience in clinical operations
• Experience leading complex global clinical projects
• Experience with CROs and regulatory authorities
• Strong written and spoken English communication

Responsibilities

• Directly manage, mentor, and develop CTMs and CTAs
• Conduct performance evaluations and provide feedback
• Ensure adequate resourcing and workload distribution
• Collaborate with Global Trial Leads (GTLs) on trial activities
• Support training initiatives across Trial Operations
• Lead process improvements and SOP development

Skills

Clinical trial leadership

Mentoring CTMs/CTAs

Resource planning

Budget planning

Regulatory knowledge

English communication

Education

Bachelor of science in a relevant field

Master of science preferred

Job description

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!

Overview

The Associate Director, Trial Delivery Team Lead plays a key leadership role in overseeing Clinical Trial Managers (CTMs) and Clinical Trial Associates (CTAs) while supporting the broader Clinical Trial Management (CTM) organization. This individual ensures high-quality clinical trial execution by providing strategic guidance, mentorship, and operational oversight. The Line Manager is responsible for team development, resource allocation, process optimization, and ensuring alignment with organizational goals and regulatory standards. The Trial Delivery Team Lead may assume Global Trial Lead (GTL) responsibilities to address fluctuating demands.

Roles & Responsibilities

Leadership and Line Management

• Directly manage, mentor, and develop Clinical Trial Managers (CTMs) and Clinical Trial Associates (CTAs), fostering professional growth.
• Conduct performance evaluations, provide feedback, and identify training and career development opportunities.
• Ensure adequate resourcing, workload distribution, and succession planning within the team.
• Facilitate cross-functional collaboration and knowledge-sharing within the clinical operations team.
• Collaborate with Global Trial Leads (GTLs) on trial activities for assigned direct reports.
• Support trial deliverables by facilitating progress, coaching, and mentoring CTMs and CTAs.
• Advise on resource needs and support overall clinical trial resource planning.
• Ensure team success through setting clear expectations, guiding performance, and leading competency development.
• Lead functional working groups; serve as process owner or Subject Matter Expert (SME) within Clinical Operations.
• Support training initiatives across Trial Operations as needed.
• Collaborate with senior leadership to define and implement best practices within the Development Operations organization.

Process & Compliance Management

• Ensure team adherence to Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements (FDA, EMA, etc.).
• Develop and refine Standard Operating Procedures (SOPs) to optimize trial efficiency and compliance.
• Support audits, inspections, and regulatory interactions by ensuring inspection readiness across clinical trials.
• Identify and drive process improvements to enhance trial execution and data quality.
• Lead cross-trial initiatives as needed, such as implementation of Corrective and Preventive Actions (CAPAs) or new process rollouts across the program.
• Manages the execution and implementation of CTM and CTA tasks, ensuring operational success.
• Initiates and supports the development of processes within the CTM and CTA group, focusing on practical application and continuous improvement.
• Collaborates across functions to drive efficiencies and provide day-to-day guidance to the CTM and CTA groups.

Requirements – what you must have

• Bachelor of science degree with relevant specialization; Master of science degree preferred
• Minimum requirement of 12 or more yearsof experience in clinical operations
• Significant experience in leading and managing complex global clinical projects/programs
• Significant experience managing/guiding internal (cross-functional) and external (CRO, regulatory authorities) teams
• Experience with operational management and budget planning
• Proven performance in earlier role/comparable role
• Global clinical program level experience required
• Experience within the field of oncologyis preferred
• Minimum 2 years’ experience as Clinical Operations representative in Clinical Development Teams (CDTs) or Global Project Teams (GPTs) would be preferable
• Experience leading team members in global matrix environment, leveraging tools and technology to ensure business needs are met.
• Strategic thinking with ability to optimize organizational resources for successful program execution
• Excellent communication skills in English, both written and spoken

Moreover, you meet the following personal requirements:

• Dedicated team player who enjoys leading teams and inspire trust among colleagues
• Quality mindset and able to prioritize your 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 as follows:

$158,720.00---$238,080.00

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.

When you join Genmab, you’re 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

Further details on eligibility for compensation and benefits based on role will be provided during the recruitment process

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, Genmab’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, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com 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 (genmab.com).

Please note that if you are applying for a position in the Netherlands, Genmab’s 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.