Senior Manager, Clinical Trial Planning
$131,040 - $196,560 per year
Key Skills
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 Senior Manager, Clinical Trial Planning is an individual contributor focused on supporting Clinical Trial Teams (CTTs) in the effective management of clinical trial timelines across the portfolio. The role drives planning system enablement (Planisware), owns and maintains a standardized Microsoft Project (MSP) trial planning template, and develops high-quality timeline visualizations to support trial execution and governance decision-making. The role partners closely with Global Trial Leaders (GTLs), who are accountable for the overall delivery of their trials and retain ownership of trial timelines within internal planning systems. The Clinical Trial Planner complements this accountability by ensuring planning data is structured, standardized, and translated into clear, actionable insights that enable effective execution and decision-making. Responsibilities/tasks Planisware Enablement & Trial Support Partner with GTLs across the portfolio to drive effective use of Planisware and ensure trial plans reflect agreed assumptions, dependencies, and execution strategy, while GTLs retain overall accountability. Liaise with Development Program Managers (DPMs) to align trial-level plans with program- and asset-level timelines and milestones. Collaborate with the Portfolio Planning team to provide structured trial-level insights and recommendations that inform ongoing refinement and maintenance of Planisware templates and standards. MS Project (MSP) Template Ownership & Standardization Develop and maintain a fit for purpose Microsoft Project (MSP) Trial Planning template for GTL use across study phases. Ensure alignment between the MSP template, Planisware, and portfolio-level planning standards. Provide guidance to GTLs to promote consistent, high-quality timeline development using the MSP template. Data Visualization Develop and deliver clear visualization templates derived from Planisware and/or MSP data, displaying key milestones and activities. Tailor visual outputs to support CTTs, governance, and leadership discussions. Process & Tool Adoption Act as a Planisware subject matter expert at the trial-support level. Reinforce GTL training through hands-on guidance and real-time coaching. Apply and promote standardized planning methodologies and visualization standards across the portfolio. Governance Awareness & Decision Support Prepare timeline views and supporting materials aligned with governance forum expectations (e.g., Project Board, Portfolio Board, Operational Review Committee). Anticipate governance triggers based on timeline changes or emerging risks. Translate planning data into concise, decision-ready visuals and summaries. Requirements/Preferences Senior Manager Bachelor’s degree required; advanced degree preferred. Approximately 7-10+ years of experience in clinical trial operations, project management, trial planning, or related roles. Demonstrated experience driving planning system adoption and influencing cross-functional stakeholders. Experience developing or standardizing planning templates, tools, or reporting frameworks across multiple studies. Strong understanding of portfolio-level planning considerations and governance expectations. Advanced analytical capability and ability to provide structured execution insight to leadership forums. For US based candidates, the proposed salary band for this position is as follows: $131,040.00---$196,560.00 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.
Core Responsibilities
Support clinical trial teams and Global Trial Leaders in effective trial timeline planning, including Planisware enablement and ownership of a standardized Microsoft Project trial-planning template. Create clear timeline visualizations and governance materials, align trial plans with program milestones, and provide coaching and decision-ready insights.
Requirements
A bachelor’s degree is required, and an advanced degree is preferred. The role seeks approximately 7–10+ years of relevant experience, with demonstrated planning-system adoption, cross-functional stakeholder influence, template or reporting standardization, portfolio-planning knowledge, and strong analytical capability.
Benefits
- 401(k) Plan
- Health Insurance
- Dental Insurance
- Vision Insurance
- Critical Illness Insurance
- Accident Insurance
- Hospital Indemnity Insurance
- Paid Vacation
- Paid Sick Leave
- Paid Holidays
- Paid Parental Leave
- Backup Care
- Family Support Programs
- Financial Wellness Tools
- Emotional Well-Being Support
- Commuter Benefits
- Tuition Reimbursement
- Lifestyle Spending Account
- Discretionary Bonuses
- Long-Term Incentives
About Genmab
Industry: Biotechnology Research
Company size: 1,001-5,000 employees
We are an international biotechnology company dedicated to improving the lives of people with cancer and other serious diseases through innovative antibody medicines. Long recognized for our expertise in antibody innovation, our passionate and collaborative team has pioneered antibody-based formats, including bispecific antibodies, antibody-drug conjugates, immune-modulating antibodies, and other modalities for the treatment of cancer and other serious diseases. Today, we are advancing a strong late-stage clinical pipeline, including wholly owned programs, with the goal of delivering transformative medicines to patients. Our quest to turn science into medicine and transform the treatment of cancer and other serious diseases is guided by our core values: a passion for innovation, determination, integrity, working as one team, and respecting each other. When you work at Genmab you'll be part of a warm, fun, dynamic community seeking out and embracing the opportunity to build new and bold futures within a rapidly growing biotechnology company. Genmab is a place where you can be authentically you; you are empowered to innovate, build solutions and execute; you feel cared for and supported. Altogether, this makes working at Genmab an extra[not]ordinary® experience. Headquartered in Copenhagen, Denmark, Genmab has a strong international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com. Disclaimer: http://gmab.ly/Jn0e50XWplA