Director - US Medical Affairs Lead

March 10

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Inogen

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Inogen is a global leader in portable oxygen technology, dedicated to innovating and improving oxygen concentrators for better patient outcomes. Since 2001, Inogen has developed multiple generations of portable oxygen concentrators (POCs), each more powerful and efficient than the last. The company's POC solutions provide flexibility and mobility to patients with oxygen therapy needs, with products offering significant battery life and ease of use. Inogen's devices are backed by peer-reviewed clinical research, ensuring their effectiveness and reliability. With a presence in over 59 countries, Inogen remains at the forefront of the global oxygen therapy market through its commitment to quality and patient-centric design.

501 - 1000 employees

Founded 2001

⚕️ Healthcare Insurance

💰 $20M Venture Round on 2012-04

📋 Description

• We are seeking Director of Medical Affairs to lead key medical and clinical affairs activities across the department. • Reporting directly to the Chief Medical Officer, this role leads the overall activities of U.S. Medical Affairs. • The role collaborates with the commercial, regulatory, sales, and operations functions. • Play a pivotal part in identifying and engaging HCPs and patient advocacy groups through collaborative partnerships to enhance educational initiatives. • Advise the medical and clinical affairs department on matters of strategic importance. • Lead business and operational planning across key medical activities including Medical Information, Medical Communications and Publication planning, and Grants and Medical Education. • Collaborate with cross-functional teams, including Clinical Operations, Marketing, and Sales. • Facilitate scientific exchange and provide education on evolving Inogen portfolio products. • Work closely with the sales organization, HMEs/DMEs to support team’s ability to understand clinical information. • Design and implement clinical training curriculums by assessing organizational, HCP, and patient advocacy requirements. • Develop a network of scientific experts and medical key opinion leaders, and other stakeholders in the respiratory field. • Establish strong relationships with relevant patient advocacy groups and identify gaps in patient education. • Respond to unsolicited inquiries from healthcare professionals regarding products, clinical trials, therapeutic area, and medical literature. • Provide scientific and clinical insights to support the development and execution of clinical trials, publications, and medical education programs. • Support scientific research and collaboration, IIR submissions and grants through appropriate internal processes.

🎯 Requirements

• Advanced degree such as RT, PhD, or PharmD in a relevant scientific discipline. • Highly desired experience in respiratory space. • Extensive knowledge of respiratory therapeutic area, including current treatment paradigms, clinical trials, and emerging trends (Preferred). • 7-10 years of experience in the pharmaceutical or biotechnology industry with relevant transferable experience e.g., licensed mental health professional, academic research etc. • Two years in a leadership/management role. • Advanced knowledge/proficiency with dashboard management, tracking and reporting on functional deliverables, and compliance tracking, required. • Proven track record of building and maintaining relationships with KOLs and other key stakeholders. • Experience developing and maintaining relationships with physician customers and field reps. • Experience with development of educational content and delivering systematic training. • Strong understanding of clinical research methodology, biostatistics, and regulatory requirements. • Excellent communication and presentation skills, with ability to effectively communicate scientific and medical information to diverse audiences. • Ability to work independently and collaboratively in a fast-paced, dynamic environment. • Advanced proficiency with Excel, Word, PowerPoint, Outlook, NCBI, Clinicaltrials.gov, FDA platforms. • A combination of training, education and experience that is equivalent to the qualifications listed above and that provides the required knowledge, skills, and abilities.