Director, Medical Affairs - Morrisville

+Liquidia Technologies is seeking a Market Access Medical Science Liaison (MAMSL) to serve as a field-based scientific and strategic expert supporting managed care, Medicaid, and specialty pharmacy stakeholders involved in the access, education, and real-world utilization of YUTR ...

The Associate Director, Regulatory Operations & Projects is responsible for managing Liquidia's regulatory operations and regulatory infrastructure projects in the planning, coordination, · & execution of global regulatory submissions, document management activities, · & evolving ...

The Head of R&D and Scientific Strategy leads medical and scientific contributions across clinical development programs and strategic partnerships in a TA. · The role will directly influence business growth through innovation and alignment. Develop strategies for exploring new in ...

Teleflex is investing in our capability to drive material cost improvement opportunities as part of a strategic corporate approach to reversing recent trends in cost escalation and generating significant stakeholder value. · ...

We have successfully supported the top pharmaceutical companies and more than 750 biotechs in the last years. · ...

We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. · We are agile and driven to accelerate the delivery of therapies, because we are passionate about changing lives. · Syn ...

The Senior Director, CMC Global Regulatory Affairs is responsible for leading all regulatory CMC development, registration, and compliance activities from early development through commercialization. · Lead development of CMC and device regulatory submission strategies by working ...

We Equip Clinicians With Some Of The Most Advanced Medical Devices On The Market Today, From Our World-class Brands Including The Arrow EZ-IO System that helps address the time-critical challenge of emergency vascular access, · and QuikClot and QuikClot Control+ hemostatic device ...

The QMS AI Quality & Compliance Specialist is responsible for supporting the implementation and operation of Thermo Fisher Scientific's AI Compliance Program within GxP-regulated environments.Apply established Quality standards, policies, and procedures to AI systems used in GxP- ...

We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Every day we perform better because of how we work together, · We bring a wide range of talented experts together across a wide range of business-critical servi ...

The VP directly influences the strategic success of the organization by delivering transformative project outcomes, fostering executive client partnerships, · fostering a culture of strategic excellence and innovation.,Provide strategic and scientific oversight for proposals. · S ...

The Therapeutic Area Segment Lead provides strategic scientific operational leadership for a defined segment within the Tx Area sub areas ensuring excellence in project delivery strengthening scientific operational rigor driving segment-level growth capability development in alig ...

This role is responsible for creating biocompatibility evaluations and overseeing testing activities as necessary to support a variety of projects related to R&D and design control changes, · as well as special projects. ...

The Clinical Quality Assurance Manager will participate in continuous improvement of the quality system framework at Science 37 by executing internal clinical quality audit plans. This position provides daily quality oversight of the conduct of clinical trials. ...

This role leads the global CRM strategy as part of the Commercial Excellence function. · ...

The Assoc. Director / Director, Clinical Development Operations will have a strong blend of scientific knowledge, clinical operations and regulatory expertise., · ,Clinical Study Strategy & Oversight: · , Partner with the clinical team to design and execute diagnostic clinical s ...

The Associate Director Regulatory Affairs – CMC is responsible for preparing regulatory submissions to support clinical development registration lifecycle management assigned project including small molecules drug-device combinations. · ...

The Senior Director of Global Marketing will lead a team to develop and implement global commercial strategies and tactics across airway & pain management, urology, and respiratory products. · ...

Join us as DIRECTOR OPERATIONS AND LEAD A MEDICAL INFORMATION CONTACT CENTER TEAM TO DEVELOP AND IMPLEMENT STRATEGIC INITIATIVES! · ...

Join us as a Director Operations and lead a medical information contact center team to develop and implement strategic initiatives, · ensure compliance with regulatory standards, manage the dissemination of accurate medical information, · Cultivate a supportive, motivating and co ...