Director, Medical Science Liaison Salary at Sunovion Pharmaceuticals Inc BETA

Medical Science Liaison (MSL) - Northeast Location: New England, NY, NJ Position Type: Full-time About the Company: We are an innovative pharmaceutical company dedicated to advancing ophthalmic care through cutting-edge therapies. Our team is passionate about improving patient outcomes, and we are seeking a highly skilled Medical Science Liaison (MSL) to join us in the Mid-Atlantic region. Role Summary: The Medical Science Liaison (MSL) will serve as a critical bridge between the company and the medical community, fostering relationships with key opinion leaders (KOLs) and healthcare professionals. This role involves delivering scientific and clinical insights, supporting educational initiatives, and contributing to the development and launch of innovative therapies. Key Responsibilities: Establish and maintain strong, credible relationships with KOLs, academic institutions, and healthcare professionals within the Mid-Atlantic territory. Provide accurate and balanced scientific informa

Job Description The Medical Patient Access Enablement Lead at Takeda focuses on enhancing customer relationship management tools and processes aligned to business requirements and priorities. This is a role with a tactical focus responsible for defining, prioritizing and managing the product backlog for specific features and releases across Medical Patient Access platforms and products. Key objectives include aligning the OPA (One Patient Access) system with medical workflows, ensuring compliance with healthcare regulations, prioritizing features that improve patient engagement and data security, and collaborating with stakeholders to deliver user-friendly, efficient, and patient-centered solutions. The Medical Patient Access Enablement Lead contributes to the OPA global product/platform roadmap based on patient services needs through close partnership with local product managers and platform team and related infrastructure. Key objectives summary: ·Deliver Medical Patient Access visio

Description: We're currently hiring for an Architect/Project Manager to support a growing studio in Harvard, MA. The ideal candidate will have 8-13 years of experience and will be licensed or on the path to licensure, and will have experience in Commercial, Industrial, Healthcare, or Life Sciences sectors. This is not a contract or part-time position. This is a full time, direct hire opportunity. As a Project Manager, you will be responsible for: Serving as the primary contact liaison Determining scope of work, estimate fees, and preparing proposals and contracts Actively manage budgets, schedules and utilization of staff to ensure efficiency and achieve project profitability Deliver projects that represent the vision of the client, and that are on time, within budget, and meet quality standards Responsible for managing and developing client relationships to promote repeat and future opportunities We're also open to considering Sr. Design applicants with 7-10 years of experience that a

At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on three therapeutic areas and other targeted investments, we push the boundaries of what is possible to bring life-changing therapies to patients worldwide. How you will contribute: OBJECTIVES: Responsible for the development and implementation of innovative device and integral/co-packaged combination product regulatory strategies for development, registration, commercialization and life cycle management of assigned asset programs in US For US and with a global mindset, utilizes technical combination product knowledge, regulatory expertise and global regulatory lessons learned to shape global regulatory best practices, drive internal consistency and influence effective change management Monitors regulatory landscape in US to maintain contemporary knowledge of global medical device and combination product regulations, stand

Job Profile Summary This role focuses on providing professional and nonprofessional nursing care services in accordance with physician orders. In addition, this role focuses on performing the following Nurse Navigator duties: Focuses on the patient's needs and helps guide the patient through the healthcare system and works to overcome obstacles that are in the way of the patient receiving the care and treatment they require. A professional individual contributor role that may direct the work of other lower level professionals or manage processes and programs. The majority of time is spent overseeing the design, implementation or delivery of processes, programs and policies using specialized knowledge and skills typically acquired through advanced education. A senior level role that requires advanced knowledge of job area typically obtained through advanced education and work experience. Typically responsible for: managing projects / processes, working independently with limited supervi

Description: PSM’s will work with patients, physician offices, partners and insurance companies to case manage all steps required to gain access to therapy. Maintain relationship with patients and physicians to ensure ongoing compliance with therapy. Works closely with patient/family to case manage all steps required to gain access to therapy Acts as the liaison with medical offices Work with Specialty Pharmacy and insurance companies to obtain reimbursement information Perform benefit investigations with insurance companies as required Counsel patient/family on reimbursement options Education: BA/BS in the life sciences or communications preferred 3 -5 years of prior case management experience preferred

Executive Director, Quality Control and Analytical Development ~ Burlington, MA ~ Local Candidates Only Please The Executive Director is accountable for overseeing all aspects of Quality Control and Analytical Development within the organization including QC systems, Analytical Chemistry, Microbiology (including Environmental Monitoring), Method Validation and Product Stability ensuring that the company QC practices comply with relevant industry standards, governmental regulations, and certifications. The Executive Director directs the development, planning, implementation, and is accountable for the Quality control methods, processes, and operations for all company development and commercial products and/or technologies. The Executive Director provides strategic and tactical leadership to the Quality Control and Analytical organization is accountable for the execution of Quality control and analytical development responsibilities within the Quality System. This position directly manag

The Medical Science Liaison (MSL) team is responsible for establishing, fostering, cultivating and maintaining relationships with HCPs with the end goal of educating and providing information on the company products, developing and building relationships with both national and regional medical thought leaders, facilitating research endeavors, and educating HCPs. In addition, the MSL provides scientific insights back to Medical Affairs management. The MSL should have an in-depth understanding of areas related to Endocrinology and Gastroenterology to support both approved and pipeline compounds. This is a front-line field position, critical to establishing and maintaining excellent educational and research collaborations with HCPs, thought leaders, investigators and key academic institutions to build outstanding product awareness and advocacy. Further, the MSL should have experience in the appropriate exchange of scientific information related to products with boxed warnings and REMS pro