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Attends and participates in monthly financial reviews, quarterly financial reviews, and other dyad-related, financial and talent planning meetings. Performs other duties as assigned and modified at the discretion of the Chief Medical Officer. A valid, active medical license in state of employment...

Demonstrates knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization and leverages this knowledge to drive improvements within Regeneron, aligned with corporate prioritie...

The Program Data Management Lead is responsible for leadership and overall strategic management of Programs in Clinical Data Management (CDM). Maintains an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or changes that may impact quality, ti...

The Program Data Management Lead is responsible for leadership and overall strategic management of Programs in Clinical Data Management (CDM). Maintains an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or changes that may impact quality, ti...

The Associate Director, Systems Management is responsible for the strategic oversight and day-to-day management of systems that support the delivery of regulated documentation to business stakeholders.This role involves maintaining the electronic Document Management System (EDMS), acting as the B...

The Manager, Vendor & Relationship Management (VRM) provides support to the operational requirements for which VRM has accountability to ensure optimal functionality and business operations within VRM along with support of the overall delivery of the Vendor Engagement life cycle. Partner with li

Providing strategic guidance on messaging and effective communications as well as the development and hands-on execution of communications tactics. In this hybrid role, you'll have a defined work location that includes work from home and a minimum eight assigned office days per month that will be...

The Senior Manager of Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases in the assigned Therapeutic Area. We will expect this to include safety data aggregation, review and analysis to support appropria...

Join the fastest-growing Academy of Early Education in the nation where "Happy Happens Here"!.At The Learning Experience, we are dedicated to providing a platform for showcasing talents, sharing ideas, and advancing careers in Early Childhood Education.We are currently seeking a passionate indivi...

Job description Position: Principal- Regulatory Change Management, Risk and ComplianceInfosys Consulting – What We DoWe are a leader in advisory services for many of the world’s best-known names in Financial Services. ...

The candidate will be leading the regulatory strategies for biologic products and combination products for the product portfolio assigned.In this role, a typical day might include the following:.Responsible for CMC/CP product development activities to lead the regulatory standpoint during early p...

To be considered for the opportunity, we expect you to have at 5 years of experience in the life science industry with a focus in biopharmaceutical manufacturing or regulatory or compliance related activities with a Bachelor's degree in Chemistry, Bio or related field. ...

Project Manager – Executive, Decks and MS Excel. ...

As a Clinical Study Lead (CSL), you will lead the cross-functional study team responsible for the global execution of large, complex clinical trials from study design through study close out.These responsibilities apply to both internally sourced studies and studies outsourced to CROs, so we need...

Additionally, ≥ 8 years of pharmaceutical clinical drug development experience. ...

The incumbent will also develop and deliver training to non-statistical colleagues, collaborate on development of new infrastructure and processes, and influence the external pharmaceutical industry and regulatory environment through participation in professional associations, conferences, and pu...

Product Manager SIM Device Management Basking Ridge, New Jersey, United States | Posted: 7/5/2024 Product Manager Device Management SIM eSIM Duration: 1 year with potential extensions Location: Onsite Hybrid in Basking Ridge New Jersey (NJ). ...

As an Associate Director of Transactional Communications, you will manage a team responsible for the design, development, and execution of transaction-driven and other non-marketing communications. When needed you will provide the team assistance on communications that need additional oversight, ...

Demonstrates knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization and leverages this knowledge to drive improvements within Regeneron, aligned with corporate prioritie...

Additionally, ≥ 8 years of pharmaceutical clinical drug development experience. ...

Minimum of 7 years experience in the biotech/pharmaceutical industry with a strong focus in Regulatory Intelligence. ...

Minimum of 5 years’ experience in the biotech/pharmaceutical industry or health authority. Experienced in the monitoring and sourcing of regulatory requirements information in pharmaceutical industry. ...

You’ll enjoy the flexibility to work remotely * from anywhere within the U. ...

Senior Sales Director Description:Responsible for identifying and closing deals in the Life Sciences spaceBe the face of Infosys to the market and help position Infosys as an industry leader and trusted advisorLeverage the Infosys ecosystem of capabilities across technology practices, industry ve...