Insmed is seeking a highly experienced and visionary Vice President to help us expand what's possible for patients with serious diseases. Candidate will lead all Chemistry, Manufacturing and Controls (CMC) activities for the company's small molecule pipeline. As a senior leader, s/he will oversee drug substance and drug product development, analytical development and combination product development. Successful applicant will ensure that development programs meet scientific, quality, regulatory and commercial standards, while ensuring execution across internal teams and external partners. More...

Incumbent will be responsible for leading day-to-day management and execution of market research projects that will help to shape U.S. commercial strategy. S/he will have the opportunity to collaborate with cross-functional teams. In addition, the individual will collaborate with cross-functional partners to identify key business questions that would benefit from market research; draft RFPs for primary market research projects; and manage market research (both qualitative and quantitative) to provide insights that support business decision making. More...

This role will be accountable to develop and maintain the high-level design plan for the overall logical and technical network and monitoring architecture. Candidate will provide technical leadership and consulting across the organization, from strategic decision making down to the project planning level. S/he will obtain organizational commitment for all high-level network and infrastructure monitoring plans and initiate and participate in projects to evaluate technologies and methods for implementing these plans. More...

This position will work closely with the executive leadership team, regulatory authorities and key external stakeholders to lead the clinical development program from pre-clinical stages through to post-market activities. S/he will act as a strategic thought leader in the field of cell and gene therapy and provide clinical expertise in the design, execution and interpretation of clinical trials, regulatory submissions and product commercialization. Applicant will interact act as a key clinical resource in interactions with regulatory agencies. More...

Applicant will contribute to internal innovation initiatives and participate in collaborations with external partners to enhance analytical workflows that support scalability, regulatory compliance and cost-effectiveness. The individual may also support business case development for new technologies that improve patient access through better product understanding and control. S/he will work closely with cross-functional teams to implement novel analytical approaches across the entire development pipeline, ensuring alignment with evolving regulatory expectations and emerging scientific advancements. More...

Incumbent will oversee and manage global Treasury activities for Legend Biotech, supporting U.S. legal entity board meeting and authorizing contract spend in the U.S. Some responsibilities will include maintaining U.S., EU and China banking relationships, such as meeting with them at least once annually; ensuring the number of banking institutions utilized are adequate based upon risk and business requirements and not excessive; and managing the overall banking fees. More...

Applicant will lead and manage cross-functional Global Security investigations across the assigned region, serving as a key representative of Novartis’ Corporate Governance in addressing internal fraud, corruption and misconduct. S/he will drive the implementation of the Anti-Falsified Medicines strategic roadmap and conduct proactive investigations to detect and prevent pharmaceutical crime, ensuring patient safety and regulatory compliance. S/he will lead impartial, fact-based investigations into “high-risk” allegations of internal misconduct. More...

The successful candidate will play a key role in supporting Clinical Trial Teams and ensuring smooth trial operations. The incumbent may be assigned various tasks to support clinical trial planning, execution and oversight of clinical trials to ensure they are conducted in compliance with regulatory requirements, Good Clinical Practice and clinical trial protocols. The Manager will work cross-functionally with study teams, investigators and vendors to ensure trial objectives are met on time and within budget. More...

The Associate Director will develop and oversee Costs of Sales and partnership arrangements. Reporting to the Senior Director, FP&A, Alliance Management and Supply Chain, the candidate will lead in providing management with meaningful and insightful analysis and own the accuracy and completeness of month-end close for Costs of Sales. S/he will also serve as the Finance Business Partner to the Supply Chain Organization in developing applicable strategic and operational plans and forecasts. More...

Applicant will blend hands-on development with technical leadership in data platform and data marketplace development, ensuring seamless integration of modern data technologies while meeting the bespoke needs of different scientific and business domains. A key focus will be on implementing data catalog and marketplace components and translating governance needs into technical solutions, ensuring that data is discoverable, accessible and compliant. Candidate will need a deep understanding of modern data marketplaces and be able to guide and implement different aspects of it. More...

This position will drive digital transformation efforts and streamline data integration across solutions in the North American Finance Organization. Candidate will play a pivotal role in building expertise of Novo Nordisk’s data structure and integrating tools, such as Anaplan, with key finance processes. S/he will act as a Solution Architect and collaborate cross-functionally to convert complex business challenges into configured solutions ensuring best value for the business. The job regularly interacts with IT and data management teams. More...

The Specialist will help in the development of plans created for regulatory submissions, including preparation, delivery, archiving and tracking of regulatory submissions to FDA and Health Canada. With direction from management, applicant will contribute to creating of SOPs, Work Instructions (WIs) and training materials required to support regulatory submission-related activities; as well as update internal processes to ensure compliance with health requirements and expectations. More...