Medical affairs jobs in Elizabeth, New Jersey (NJ) State

As part of our expanding US Medical Affairs (USMA) team, Genmab is seeking a Senior Director, USMA Solid Tumor Portfolio. This role will report to the VP/Head of US Medical Affairs and will be responsible for building and leading the USMA team for the solid tumor portfolio. Builds, leads and over...

This role primarily focuses on late-stage pipeline and marketed products, interfaces with cross-functional teams including US medical affairs, marketing, market access global value and access teams, commercial to align strategies in customer research activities and development of external communi...

Join our client's team as a Medical Director, Medical Affairs, where you will provide medical, scientific, strategic, and operational leadership. Job Title: Medical Director, Medical Affairs. Initiate and lead medical affairs activities, data generation, and dissemination to support the overall m...

The Associate Director, Field Medical Training will be responsible for the development, implementation, and continuous improvement of a strategic and comprehensive training curricula for Medical Science Liaisons (MSL), Health Outcomes Liaisons (HOL) and other Medical Affairs Employees and Conting...

The Vice President, Medical Affairs is responsible for leading the development and execution of strategic and tactical plans for Headquarter (HQ) and Field medical affairs teams pre-launch, launch, and post approval for biosimilars and biologic products. Strong, motivational leader who builds and...

The Scientific Director for US Medical Affairs in CNS/Psychiatry provides specialist medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions; evidence generation of clinical and scientific data e. Deve...

US medical affairs, HEOR, marketing, market access, global value and access teams, commercial) to prioritize projects toward achieving effective utilization of resources. The base salary range for the Director, Real World Evidence, Global Medical Affairs is from :213,500-280,200Under current guid...

The Medical Director (Medical Affairs) will report into the Medical Affairs Department and is responsible for clinical support and consultative activities across the PBM. The Medical Director (Medical Affairs) will report into the Medical Affairs Department and is responsible for clinical support...

This role primarily focuses on late-stage pipeline and marketed products, interfaces with cross-functional teams including US medical affairs, marketing, market access global value and access teams, commercial to align strategies in customer research activities and development of external communi...

The Medical Director (Medical Affairs) will report into the Medical Affairs Department and is responsible for clinical support and consultative activities across the PBM. The Medical Director (Medical Affairs) will report into the Medical Affairs Department and is responsible for clinical support...

In partnership with cross functional global medical affairs, they will support the design and implementation of the US integrated medical plan. Excellent analytical skills and solid experience in translating medical/clinical information into medical affairs strategies, with a robust understanding...

As part of our expanding US Medical Affairs (USMA) team, Genmab is seeking a Senior Director, USMA Solid Tumor Portfolio. This role will report to the VP/Head of US Medical Affairs and will be responsible for building and leading the USMA team for the solid tumor portfolio. Builds, leads and over...

The Associate Scientific Director will provide scientific/medical leadership and support to the execution and implementation of USMA strategies for the Multiple Myeloma Cell Therapy franchise by representation in cross-functional teams, and collaboration within global medical affairs. Excellent a...

The assignment involves receiving and reprocessing Reusable Medical Equipment which will be used by various customers within the medical center for scheduled or emergency procedures. Working knowledge of medical terminology, anatomy and physiology, microbiology, medical conditions and procedures....

In this role, the regulatory leader will be primarily responsible for the development of US regulatory strategies and have the role of Global Regulatory Strategist to advance Genmab’s portfolio of development and marketed drugs. Genmab is looking for an experienced and passionate leader to be a p...

RFPs)• lead collaborative engagements with external stakeholders to develop Financial Advisor education initiatives and identification of market opportunities • consistently find ways to understand client needs / competitive landscape so as to expand and enhance the program to make it easier to d...

The primary purpose of the Executive Director Clinical Diagnostic Services is to be responsible for the overall operations of the Radiology, Cardiology, Cardiothoracic Surgery, Pain Management and Neurodiagnostic testing, and treatment services offered by University Hospital. The Executive Direct...

The primary purpose of the Medical Office Assistant position is to provide support with the daily activities of the clinic including answering phones and routing calls, scheduling appointments, patient referrals, greeting and registering patients. Experience in medical office setting including so...

Lead new projects from inception through go live, managing the project lifecycle across authoring project initiation documents, business requirements documents, status reports, leading front to back UAT across users and developers. Capital Markets as a Project Manager or Business Analyst with exp...

The CUSO/IHC Local Regulatory Reporting Department is seeking a Vice President to assist in the implementation of the required regulatory reports submitted to the Federal Reserve Bank, and other regulators. Responsibilities: ·         Assist in maintaining and enhancing the BAU production process...

Two years of proven experience in scientific or medical affairs at a biotech or pharmaceutical companyAt least two years in a Medical Science Liaison roleThree or more years of clinical practice, clinical research, or medical research. Medical Science Liaison, IgG4 - Rare DiseaseLiveWhat you will...

Specialist, Site Supply Chain Compliance is responsible for the coordination, communication, management and support of various projects and information within the Site Supply Chain Compliance Team. Manage projects and compliance initiatives which directly support network and GxP initiatives, to e...

Starting on day one of your employment, you’ll be offered several health-related benefits including medical, vision, dental, and well-being and behavioral health programs. For all roles, PSEG’s drug and alcohol testing program includes pre-employment testing, testing for cause, and post-incident/...

Regulatory Affairs SpecialistPosition This hire will be a member of the Firm’s Regulatory group which is responsible for exam oversight, branch inspections, regulatory change tracking, governance related tasks and additional ad-hoc tasks. The Firm’s Regulatory Group is housed within its Legal Dep...