Genmab
Join to apply for the
Associate Director, Global Trial Lead
role at
Genmab Join to apply for the
Associate Director, Global Trial Lead
role at
Genmab Get AI-powered advice on this job and more exclusive features. 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.
The following information aims to provide potential candidates with a better understanding of the requirements for this role.
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 Global Trial Lead (GTL) is accountable for the end-to-end delivery of one or more clinical trials, from initial strategy to Clinical Study Report (CSR) completion. This includes leading cross-functional Clinical Trial Teams (CTT), managing budgets, and leveraging matrix leadership to align internal and external stakeholders in achieving trial goals efficiently and to high-quality standards. The GTL serves as the main coordinator for the Trial Team and may take on Clinical Trial Manager (CTM) responsibilities if no CTM is assigned.
Roles & Responsibilities
Trial Leadership and Management
Lead the cross functional Clinical Trial Team (CTT) including roles such as Medical, Biostatistics, Programming, and Data Management. Lead the operational Trial Team, including roles such as Start-up Specialists, Clinical Trial Associates (CTA), and Clinical Trial Managers (CTM). Manages CTT resources/membership, assign tasks, and ensure deadlines are met. Make tactical decisions within scope to ensure that CTT work aligns with program objectives. Define and manage CTT goals in collaboration with team members. Provide regular updates, reports, and escalations to the DOPL regarding progress, challenges, risks, and resource needs. Review and approve key trial documents, including protocols, amendments, plans, and manuals. Oversee vendor selection and manage trial-related contracts and amendments. Drive country selection and coordinate responses to IEC/IRB comments. Maintain trial integrity by ensuring protocol adherence and addressing data trends. Collaborate with the Development Operations Program Lead (DOPL) on cross-functional clinical development team activities and escalate issues as needed. Execute strategies for drug supply, regulatory submissions, and patient recruitment.
Budget and Planning
Assist in the development and management of the trial budget. Plan and maintain integrated trial timelines from study outline through CSR. Develop recruitment projections and approve adjustments as needed with the Project Lead. Act as counterpart to the CRO Project Lead/Manager.
Risk Management
Identify and manage trial risks with the CTT. Oversee maintenance of CTT issue, action and decision logs. Assist in audit preparation and ensure corrective and preventive actions (CAPAs) are implemented. Act as Subject Matter Expert (SME) for processes within Clinical Operations
Core Skills And Competencies
Required experience working in a complex, global and matrixed organization
Required Pharmaceutical Industry Experience With Knowledge Of ICH/GCP Regulations
Required oncology or TA specific drug development experience and various phases of development
Required Experience Mentoring Others
Required matrix leadership experience (ability to lead without authority)
Proven leadership experience with a strong focus on people management and developing others preferred
Expected To Have Advanced Knowledge In
End-to-end trial planning and execution
Outsourcing and vendor management.
Expected To Be Proficient In
Project management skills and knowledge of tools and processes Regulatory submission knowledge Develop and monitor key performance metrics Excellent written and verbal communication skills Excellent negotiation, collaboration and interpersonal skills with ability to work effectively with others at all levels of the organization Strong trial planning and budget management skills. Strong understanding of clinical trial processes, ICH-GCP regulations, and the clinical drug development lifecycle Ability to proactively identify risks, develop mitigation strategies, and resolve issues effectively. Experience managing trials in global settings, with the ability to oversee complex, multi-regional operations. Stakeholder management skills.
Learning and developing strong program planning and budget management skills.
Developing ability to drive working groups and lead process improvements, champion more efficient and effective methods/processes
For US based candidates, the proposed salary band for this position is as follows:
$148,320.00---$222,480.00
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
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 you’re 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, 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.Seniority level
Seniority levelDirector Employment type
Employment typeFull-time Job function
Job functionBusiness Development and Sales Referrals increase your chances of interviewing at Genmab by 2x Assistant Manager/Assistant Director/Fitness Director/ PT Director West Windsor, NJ $12,000.00-$49,500.00 2 weeks ago Assistant Director, Strategic Operations New Jersey, United States $81,850.00-$106,400.00 4 days ago Associate Director, Patient Support - Job ID: SMPS Princeton, NJ $155,000.00-$170,000.00 1 month ago Associate Director, Consumer Insights, VINCI New Jersey, United States $137,000.00-$226,500.00 1 week ago Associate Director, Global Strategic Marketing - Job ID: 1649 Princeton, NJ $170,000.00-$190,000.00 1 month ago Business Development Roles - East Coast (Director to Senior Director) Piscataway, NJ $170,000.00-$200,000.00 1 week ago Associate Director, Global Scientific Training - Job ID: ADGST Princeton, NJ $180,000.00-$195,000.00 4 days ago Associate Director, Procurement, Excellence & PerformanceAssociate Manager, Training & Communications, HOKA NA Retail Branchburg, NJ $134,250.00-$196,900.00 4 days ago Senior Director/Director of Study Start-up Princeton, NJ $180,000.00-$220,000.00 4 days ago Associate Director - Strategic CollaborationAssociate Director, Regional Marketing & Product Management, Catalog Products Piscataway, NJ $90,000.00-$140,000.00 1 week ago Princeton, NJ $210,000.00-$285,000.00 1 week ago Associate Director, HRBP - HOCT & Early DevelopmentAssociate Director, US CV/IMM Commercial FinanceAssociate Director, Global Publication Planning - Job ID: ADGPP Princeton, NJ $170,000.00-$185,000.00 3 weeks ago Plainsboro, NJ $148,290.00-$259,510.00 5 hours ago Princeton, NJ $102,000.00-$138,000.00 1 day ago Burlington, NJ $150,000.00-$190,000.00 6 days ago Lawrenceville, NJ $90,000.00-$110,000.00 2 weeks ago Senior Director, Head of US Patient and Professional Advocacy Princeton, NJ $272,000.00-$292,000.00 1 week ago Plainsboro, NJ $148,290.00-$259,510.00 2 weeks ago Associate Director, Commercial Finance, U.S. Cell TherapyAssociate Director - Academy & Franchise, Employee Experience Plainsboro, NJ $116,810.00-$216,100.00 2 weeks ago Senior Director, Strategy & Operations - MAx We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr
Associate Director, Global Trial Lead
role at
Genmab Join to apply for the
Associate Director, Global Trial Lead
role at
Genmab Get AI-powered advice on this job and more exclusive features. 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.
The following information aims to provide potential candidates with a better understanding of the requirements for this role.
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 Global Trial Lead (GTL) is accountable for the end-to-end delivery of one or more clinical trials, from initial strategy to Clinical Study Report (CSR) completion. This includes leading cross-functional Clinical Trial Teams (CTT), managing budgets, and leveraging matrix leadership to align internal and external stakeholders in achieving trial goals efficiently and to high-quality standards. The GTL serves as the main coordinator for the Trial Team and may take on Clinical Trial Manager (CTM) responsibilities if no CTM is assigned.
Roles & Responsibilities
Trial Leadership and Management
Lead the cross functional Clinical Trial Team (CTT) including roles such as Medical, Biostatistics, Programming, and Data Management. Lead the operational Trial Team, including roles such as Start-up Specialists, Clinical Trial Associates (CTA), and Clinical Trial Managers (CTM). Manages CTT resources/membership, assign tasks, and ensure deadlines are met. Make tactical decisions within scope to ensure that CTT work aligns with program objectives. Define and manage CTT goals in collaboration with team members. Provide regular updates, reports, and escalations to the DOPL regarding progress, challenges, risks, and resource needs. Review and approve key trial documents, including protocols, amendments, plans, and manuals. Oversee vendor selection and manage trial-related contracts and amendments. Drive country selection and coordinate responses to IEC/IRB comments. Maintain trial integrity by ensuring protocol adherence and addressing data trends. Collaborate with the Development Operations Program Lead (DOPL) on cross-functional clinical development team activities and escalate issues as needed. Execute strategies for drug supply, regulatory submissions, and patient recruitment.
Budget and Planning
Assist in the development and management of the trial budget. Plan and maintain integrated trial timelines from study outline through CSR. Develop recruitment projections and approve adjustments as needed with the Project Lead. Act as counterpart to the CRO Project Lead/Manager.
Risk Management
Identify and manage trial risks with the CTT. Oversee maintenance of CTT issue, action and decision logs. Assist in audit preparation and ensure corrective and preventive actions (CAPAs) are implemented. Act as Subject Matter Expert (SME) for processes within Clinical Operations
Core Skills And Competencies
Required experience working in a complex, global and matrixed organization
Required Pharmaceutical Industry Experience With Knowledge Of ICH/GCP Regulations
Required oncology or TA specific drug development experience and various phases of development
Required Experience Mentoring Others
Required matrix leadership experience (ability to lead without authority)
Proven leadership experience with a strong focus on people management and developing others preferred
Expected To Have Advanced Knowledge In
End-to-end trial planning and execution
Outsourcing and vendor management.
Expected To Be Proficient In
Project management skills and knowledge of tools and processes Regulatory submission knowledge Develop and monitor key performance metrics Excellent written and verbal communication skills Excellent negotiation, collaboration and interpersonal skills with ability to work effectively with others at all levels of the organization Strong trial planning and budget management skills. Strong understanding of clinical trial processes, ICH-GCP regulations, and the clinical drug development lifecycle Ability to proactively identify risks, develop mitigation strategies, and resolve issues effectively. Experience managing trials in global settings, with the ability to oversee complex, multi-regional operations. Stakeholder management skills.
Learning and developing strong program planning and budget management skills.
Developing ability to drive working groups and lead process improvements, champion more efficient and effective methods/processes
For US based candidates, the proposed salary band for this position is as follows:
$148,320.00---$222,480.00
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
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 you’re 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, 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.Seniority level
Seniority levelDirector Employment type
Employment typeFull-time Job function
Job functionBusiness Development and Sales Referrals increase your chances of interviewing at Genmab by 2x Assistant Manager/Assistant Director/Fitness Director/ PT Director West Windsor, NJ $12,000.00-$49,500.00 2 weeks ago Assistant Director, Strategic Operations New Jersey, United States $81,850.00-$106,400.00 4 days ago Associate Director, Patient Support - Job ID: SMPS Princeton, NJ $155,000.00-$170,000.00 1 month ago Associate Director, Consumer Insights, VINCI New Jersey, United States $137,000.00-$226,500.00 1 week ago Associate Director, Global Strategic Marketing - Job ID: 1649 Princeton, NJ $170,000.00-$190,000.00 1 month ago Business Development Roles - East Coast (Director to Senior Director) Piscataway, NJ $170,000.00-$200,000.00 1 week ago Associate Director, Global Scientific Training - Job ID: ADGST Princeton, NJ $180,000.00-$195,000.00 4 days ago Associate Director, Procurement, Excellence & PerformanceAssociate Manager, Training & Communications, HOKA NA Retail Branchburg, NJ $134,250.00-$196,900.00 4 days ago Senior Director/Director of Study Start-up Princeton, NJ $180,000.00-$220,000.00 4 days ago Associate Director - Strategic CollaborationAssociate Director, Regional Marketing & Product Management, Catalog Products Piscataway, NJ $90,000.00-$140,000.00 1 week ago Princeton, NJ $210,000.00-$285,000.00 1 week ago Associate Director, HRBP - HOCT & Early DevelopmentAssociate Director, US CV/IMM Commercial FinanceAssociate Director, Global Publication Planning - Job ID: ADGPP Princeton, NJ $170,000.00-$185,000.00 3 weeks ago Plainsboro, NJ $148,290.00-$259,510.00 5 hours ago Princeton, NJ $102,000.00-$138,000.00 1 day ago Burlington, NJ $150,000.00-$190,000.00 6 days ago Lawrenceville, NJ $90,000.00-$110,000.00 2 weeks ago Senior Director, Head of US Patient and Professional Advocacy Princeton, NJ $272,000.00-$292,000.00 1 week ago Plainsboro, NJ $148,290.00-$259,510.00 2 weeks ago Associate Director, Commercial Finance, U.S. Cell TherapyAssociate Director - Academy & Franchise, Employee Experience Plainsboro, NJ $116,810.00-$216,100.00 2 weeks ago Senior Director, Strategy & Operations - MAx We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr