Current jobs related to Director, Compound Development Program Lead - Plainsboro, New Jersey - Genmab
-
Director of Biostatistics
1 month ago
Plainsboro, New Jersey, United States Genmab Full timeAbout the RoleWe are seeking a highly skilled Director of Biostatistics to join our team at Genmab. As a key member of our clinical development team, you will play a critical role in supporting the development of innovative antibody products and therapies.Key ResponsibilitiesAct as a statistical expert supporting the clinical development of compounds,...
-
Director of Biostatistics
4 weeks ago
Plainsboro, New Jersey, United States Genmab Full timeAbout the RoleWe are seeking a highly skilled Director of Biostatistics to join our team at Genmab. As a key member of our clinical development team, you will play a critical role in supporting the development of our innovative antibody products.Key ResponsibilitiesAct as a statistical expert supporting the clinical development of compounds, including early...
-
Plainsboro, New Jersey, United States Genmab Full timeAbout the RoleGenmab is seeking a highly experienced Director, Biostatistics and Clinical Development Lead to join our team. As a key member of our clinical development team, you will be responsible for providing statistical expertise to support the development of our innovative antibody therapeutics.Key ResponsibilitiesCompound/Indication LevelAct as lead...
-
Director of Biostatistics
2 weeks ago
Plainsboro, New Jersey, United States Genmab Full timeJob DescriptionAt Genmab, we're committed to building innovative futures together, by developing antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases. Our team is passionate about our purpose and genuinely cares about our mission to transform the lives of patients through...
-
Director of Biostatistics
4 weeks ago
Plainsboro, New Jersey, United States Genmab Full timeAbout the RoleWe are seeking a highly skilled Director of Biostatistics to join our team at Genmab. As a key member of our clinical development team, you will play a critical role in supporting the development of our innovative antibody products.Key ResponsibilitiesAct as a statistical expert supporting the clinical development of compounds, including early...
-
Global Program Leader
2 weeks ago
Plainsboro, New Jersey, United States Genmab Full timeJob Title: Senior Director, Global Program LeaderGenmab is seeking an experienced Senior Director, Global Program Leader to drive the strategy and execution of 1-2 clinical stage development programs. This leadership position will be based in Princeton, NJ, with partial remote work.Key Responsibilities:Develop and execute compound strategies, working in...
-
Associate Director, Biostatistics
2 weeks ago
Plainsboro, New Jersey, United States Genmab Full timeAbout the RoleGenmab is seeking a highly skilled Associate Director, Biostatistics to join our team. As a key member of our biostatistics department, you will play a critical role in supporting the clinical development of compounds and contributing to clinical development strategies and plans.Key Responsibilities:Lead and collaborate with cross-functional...
-
Senior Clinical Research Scientist
2 weeks ago
Plainsboro, New Jersey, United States Genmab Full timeAbout the RoleGenmab is seeking a highly skilled and experienced Senior Clinical Research Scientist to join our Medical department. As a key member of our team, you will contribute to the implementation of our global development strategy, leading or co-leading one or more clinical trials in a therapeutic area for one or more compounds in various stages of...
-
Director, Regulatory Affairs Strategy Lead
1 month ago
Plainsboro, New Jersey, United States Genmab Full timeAbout the RoleWe are seeking an experienced and passionate leader to join our Global Regulatory Affairs (GRA) organization at Genmab. As a key member of our team, you will be responsible for developing and implementing global and US regulatory strategies to advance our portfolio of development pipeline candidate drugs.Key ResponsibilitiesAct as the US/Global...
-
Plainsboro, New Jersey, United States Genmab Full timeJob DescriptionAt Genmab, we're committed to building extraordinary futures together, by developing innovative antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in...
-
Director, Regulatory Affairs Strategy NJ
3 weeks ago
Plainsboro, New Jersey, United States Genmab Full timeJob DescriptionGenmab is seeking an experienced and passionate leader to join our Global Regulatory Affairs (GRA) organization as a Director, Regulatory Affairs Strategy NJ. In this role, you will be responsible for developing and implementing global and US regulatory strategies to advance Genmab's portfolio of development pipeline candidate drugs.Key...
-
Plainsboro, New Jersey, United States Novo Nordisk Full timeJob DescriptionJob Title: Associate Director, Rare Disease Portfolio LeadJob Summary:We are seeking an experienced Associate Director to lead our Rare Disease Portfolio in the United States. The successful candidate will be responsible for developing and executing commercial strategies to drive business growth and improve patient outcomes.Key...
-
Plainsboro, New Jersey, United States Genmab Full timeAbout the RoleGenmab is seeking a highly skilled and experienced Director to lead the development and execution of the Global Medical Affairs strategic and tactical plans for our robust and diverse antibody products in immuno-oncology and beyond.Key ResponsibilitiesLead annual medical planning for our assets and work closely with extended medical affairs...
-
Plainsboro, New Jersey, United States Genmab Full timeJob SummaryWe are seeking an experienced Associate Director to join our team at Genmab, a leading biotechnology company dedicated to developing innovative antibody therapeutics. As an Associate Director, Signal Detection and Management, you will play a critical role in implementing signal management group surveillance strategies for proactive and systematic...
-
Plainsboro, New Jersey, United States Genmab Full timeJob DescriptionAt Genmab, we're committed to building extraordinary futures together, by developing innovative antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases.We're seeking a highly skilled and experienced Director, Global Medical Affairs Strategy and Development to join our...
-
Global Regulatory Strategy Lead
2 months ago
Plainsboro, New Jersey, United States Genmab Full timeJob DescriptionAt Genmab, we're committed to building extraordinary futures together, by developing innovative antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases.We're looking for an experienced and passionate leader to be a part of our Global Regulatory Affairs organization....
-
Lead Qliksense Developer
2 weeks ago
Plainsboro, New Jersey, United States Lorven Technologies, Inc. Full timeJob Title: Lead Qliksense DeveloperLocation: Plainsboro, NJ (Onsite)Job Type: Contract 12+ Months (No third Party, W2 only)Job Description:We are seeking a skilled Qliksense Developer to lead our team in creating and managing BI and analytics solutions that turn data into knowledge. The ideal candidate should have a background in data and business analysis,...
-
Director, Biostatistics
2 weeks ago
Plainsboro, New Jersey, United States Genmab Full timeJob Title: Director, BiostatisticsGenmab is seeking a highly skilled Director, Biostatistics to join our team. As a key member of our clinical development team, you will be responsible for leading the statistical analysis and interpretation of clinical trial data.Key Responsibilities:Lead the development of statistical analysis plans and protocols for...
-
Medical Director
5 days ago
Plainsboro, New Jersey, United States Novo Nordisk Full timeAbout the RoleThe Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is a diverse and collaborative group within the organization. We are seeking a highly skilled Medical Director to join our team and contribute to the design, implementation, and monitoring of clinical studies.Key ResponsibilitiesProvide medical and scientific input to...
-
Medical Director
5 days ago
Plainsboro, New Jersey, United States Novo Nordisk Full timeThe Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is a dynamic and collaborative group within the organization.As a Medical Director, you will be involved in various aspects of clinical research and development, including health-care-provider interactions, regulatory strategies, medical education, and data collection.You will help...
Director, Compound Development Program Lead
2 months ago
At Genmab, we're committed to building extraordinary futures together, by developing innovative antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose.
Genmab is continuing its rapid growth and development, striving towards its goal of improving the lives of patients with unmet medical needs. Genmab is seeking an experienced Senior Director, Late-Stage Development Team Lead for our antibody product development programs. This is a leadership position within Genmab, accountable for driving the strategy and execution of 1-2 clinical stage development programs. This position will be based in the US with partial remote work.
The Senior Director, Late-Stage Development Team Lead will drive the development and execution of late development/marketed product development strategy(ies). The Senior Director will lead a cross-functional, matrixed team(s) to deliver against the program strategy. You will champion the program(s) at all levels of Genmab by providing clear communication, creative strategic approaches to development, and collaboration with key stakeholders. This position reports directly to the Chief Medical Officer at Genmab.
Key Responsibilities- Lead the Compound Development Team (CDT) for a late-stage co-developed program with two or more indications
- Construct asset development plans through BLA approval by leading cross-functional efforts to evaluate available data, competitive landscape, opportunity, regulatory precedence, and clinical study designs that deliver value
- Partner with Medical, Commercial, Regulatory, and Medical Affairs leaders on the CDT to problem solve and drive key workstreams balancing risk acceptability and expeditious delivery
- Direct and redirect cross-functional efforts, prioritize workstreams, and/or identify subteam needs to ensure deliverables are aligned with the big picture
- Support the CDT by providing clear communication, eliminating obstacles, and driving efficiencies that enable on time delivery and promote effective Team performance
- Drive LCM strategies that support future value of a late-stage asset through LoE
- Key contributor for all health authority engagements and externally facing efforts to 'prepare the market' including publications, corporate communications, and advisory boards
- Ensure CDT and Company goals are aligned across subteams and with individual team goals; coach and guide Team members and provide input on performance
- Continuous evaluation of CDT performance, capabilities, and needs; work with functional line management to secure required resource for project success and to influence optimal team composition
- Development Lead and face of Genmab for partnered programs ensuring development obligations within the collaboration are met, aligning on development strategy and driving joint decision making for the asset
- Lead presentation and discussion for all Stage Gate decisions, updates, and communications to governance and leadership teams, aligning with Joint governance decision making as needed
- Partner with Alliance Management on collaboration program requirements and communication needs
- Accountable for overall budget and project plan deliverables, working closely with Project Management Team members to ensure alignment on budget, resource, and timelines
- Partner with Project Management team member(s) to ensure execution against strategy, track progress, and communicate effectively within the team and organizationally
- Bachelor's degree in the life sciences is required; advanced degree is preferred
- Minimum of 15 years of experience in the pharmaceutical/biotechnology industry
- Leadership of a cross-functional oncology drug development teams with working knowledge across multiple R&D functions (preclinical, clinical, regulatory, CMC)
- Late-stage clinical development through new product launch experience, partnering with commercial and medical affairs
- Hematology experience is a plus
- Hands on BLA/NDA submission experience required
- Solid business acumen and understanding of financial concepts
- Experience working within alliances or with collaboration partners
- Strategic agility: ability to pivot a team based on emerging and/or incomplete data, business drivers, or competitive landscape
- Independent ability to manage ambiguity and to translate the big picture into specific short- and long-term deliverables
- Demonstrated ability to influence and negotiate across the organization without direct reporting authority
- Outstanding communication skills
The proposed salary band for this position is as follows:
$240,000.00 - $400,000.00
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 bonuses.
