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Genmab
Senior Clinical Trial Manager
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What they do
A Clinical Trial Manager is responsible for planning and managing all aspects of an organization's program of clinical trials, usually for an organization undertaking pharmacological drug testing.
$176,154 / year median in New Jersey
Job Description
検索結果に戻る 前職 次の仕事 仕事内容 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! About the Role At Genmab, we're dedicated to developing and delivering innovative antibody-based therapeutics to improve the lives of patients. As a Senior Clinical Trial Manager (CTM), you will play a pivotal role in driving the success of our clinical trials through strategic oversight, operational excellence, and cross-functional collaboration. The Senior CTM partners closely with Clinical Trial Teams (CTTs), service providers, and investigators to ensure that our clinical studies are executed on time, within budget, and in full compliance with regulatory standards and Genmab's high-quality expectations. This role offers the opportunity to work in a dynamic, global, and matrixed environment where you will be empowered to take ownership and lead with autonomy. Key Responsibilities Lead the operational planning, setup, and execution of global clinical trials, ensuring delivery on time, and in compliance with regulatory and quality standards. Oversee trial documentation and systems, ensuring accuracy, completeness, and continuous inspection readiness. Drive site feasibility, selection, and activation strategies in collaboration with CROs and internal stakeholders. Manage and oversee CROs and other service providers, ensuring high-quality deliverables, adherence to timelines, and effective collaboration. Proactively identify, assess, and mitigate operational risks using risk-based quality management approaches. Oversee protocol deviations, issue management, and ensure appropriate escalation and resolution of trial-level challenges. Monitor trial performance and data quality, leveraging key metrics to drive decision-making and continuous improvement. Act as a key cross-functional leader, fostering strong collaboration across internal teams, vendors, and investigators. Qualifications Bachelor's degree in life sciences or related field (Master's degree preferred). 8+ years of experience in clinical trial management within the pharmaceutical or biotechnology industry. Solid understanding of ICH/GCP regulations and the clinical drug development lifecycle. Proven experience managing global, multi-center trials and working in a complex, matrixed organization. Strong project management and service provider oversight skills. Excellent communication, collaboration, and interpersonal skills. Oncology and/or therapeutic area-specific experience is highly desirable. Ability to lead without authority and mentor others in a cross-functional environment. For US based candidates, the proposed salary band for this position is as follows: $130,720.00---$196,080.00 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.