Current jobs related to Senior Director, Field Medical Affairs - Cambridge - Apnimed
-
Senior Director of Clinical Affairs
2 weeks ago
Cambridge, Massachusetts, United States Philips Full timeJob TitleSenior Director of Clinical AffairsJob SummaryWe are seeking a highly experienced and skilled Senior Director of Clinical Affairs to join our team at Philips. As a key member of our organization, you will be responsible for delivering clinical knowledge, experience, and expertise across the entire value chain from ideation to end-of-life.Key...
-
Scientific Director for Medical Affairs
7 days ago
Cambridge, Massachusetts, United States AbbVie Full time{"title": "Scientific Director for Medical Affairs", "content": "Job SummaryWe are seeking a highly skilled Scientific Director for Medical Affairs to join our team at AbbVie. As a key member of our Medical Affairs department, you will be responsible for ensuring scientific pull-through of key medical strategies into communications across multiple...
-
Senior Director of Regulatory Affairs
9 hours ago
Cambridge, Massachusetts, United States Apnimed Full timeJob Title: Senior Director, Regulatory AffairsApnimed is a clinical-stage pharmaceutical company dedicated to transforming the treatment of sleep apnea. We are seeking a highly experienced Senior Director of Regulatory Affairs to play a key role in advancing our innovative programs through clinical trials and commercialization globally.Key...
-
Senior Director of Regulatory Affairs
7 days ago
Cambridge, Massachusetts, United States Apnimed Full time{"title": "Senior Director of Regulatory Affairs", "content": "Job SummaryApnimed is seeking a highly experienced Senior Director of Regulatory Affairs to lead the development and execution of regulatory strategies to support the approval and commercialization of our therapies globally.This is a key role in advancing our innovative programs through clinical...
-
Cambridge, Massachusetts, United States Moderna Therapeutics Full timeAbout the RoleThe Senior Manager of Medical Writing and Regulatory Affairs is a critical position within our Clinical Development team at Moderna Therapeutics. Reporting directly to the Associate Director, Director of Medical Writing, or Senior Director of Medical Writing, this individual will play a pivotal role in delivering high-quality clinical and...
-
Cambridge, United States Biogen Full timeJob DescriptionJob DescriptionJob DescriptionMedical Director, US Medical Affairs, Alzheimer's (Specialty Care)About This RoleThe Medical Director – Alzheimer’s role is a part of Specialty Care, North America (US) Medical, a strategic partner within Biogen, that helps inform medical practice across our therapeutic areas and pipeline to improve...
-
Director of Dermatology Medical Affairs
23 hours ago
Cambridge, Massachusetts, United States Takeda Full timeAbout the RoleWe are seeking a highly skilled and experienced Director of Dermatology Medical Affairs to join our team at Takeda. As a key member of our US Medical Affairs organization, you will be responsible for developing and executing medical strategies for our dermatology products.Key ResponsibilitiesDevelop and execute medical strategies for assigned...
-
Scientific Director, Medical Affairs Lead
7 days ago
Cambridge, Massachusetts, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled Scientific Director to lead our Medical Affairs team in the development and execution of strategic initiatives for our Parkinson's Disease asset. The successful candidate will provide medical and scientific input into core medical affairs activities, work closely with commercial teams, and execute core medical...
-
Senior Director, Regulatory Affairs
1 week ago
cambridge, United States Apnimed Full timeApnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...
-
Senior Director, Regulatory Affairs
3 weeks ago
cambridge, United States Apnimed Full timeApnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...
-
Senior Director, Regulatory Affairs
3 weeks ago
Cambridge, United States Apnimed Full timeApnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...
-
Senior Director, Regulatory Affairs
3 weeks ago
Cambridge, United States Apnimed Full timeApnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...
-
Cambridge, Massachusetts, United States AAPC Full time{"Job Title": "Associate Director, Medical Affairs, Adult Cholestatic Diseases", "Job Summary": "We are seeking a highly skilled Associate Director to join our Medical Affairs team in Cambridge, MA. As a key member of our team, you will be responsible for contributing to the medical strategies and overall US medical affairs plan for adult cholestatic...
-
Cambridge, Massachusetts, United States Apnimed Full timeAbout the RoleWe are seeking a highly experienced Senior Director to lead our Regulatory Affairs and Compliance team at Apnimed. As a key member of our leadership team, you will play a critical role in advancing our innovative sleep apnea treatments through clinical trials and commercialization globally.Key ResponsibilitiesRegulatory Strategy and Planning:...
-
Scientific Director, Medical Affairs
2 weeks ago
Cambridge, Massachusetts, United States AbbVie Full timeAbout the RoleAt AbbVie, we are seeking a highly skilled and experienced Associate Scientific Director, Medical Affairs to join our team. This is a key role that will provide medical and scientific strategic and operational input into core medical affairs activities.Key ResponsibilitiesContribute to the development of brand strategies with oversight.Lead and...
-
Cambridge, Massachusetts, United States Apnimed Full timeJob SummaryWe are seeking a highly experienced Senior Director to lead our Regulatory Affairs and Compliance team at Apnimed. As a key member of our leadership team, you will be responsible for developing and executing regulatory strategies to support the approval and commercialization of our therapies globally.Key ResponsibilitiesRegulatory Strategy and...
-
Scientific Director of Medical Affairs
6 days ago
Cambridge, Massachusetts, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled Associate Scientific Director to join our Medical Affairs team at AbbVie. As a key member of our team, you will provide strategic and operational input into core medical affairs activities, working closely with commercial teams to provide strategic medical input into core brand strategies.Key...
-
Cambridge, Massachusetts, United States AAPC Full timeAbout the RoleWe are seeking a highly skilled Associate Director, Medical Affairs, Adult Cholestatic Diseases to join our team at AAPC. As a key member of our Medical Affairs department, you will play a critical role in supporting and overseeing medical affairs activities for adult cholestatic therapeutic areas.Key ResponsibilitiesContribute to and lead...
-
Medical Director, Immunology
2 months ago
Cambridge, United States Biogen Full timeJob DescriptionJob DescriptionJob DescriptionMedical Director, Immunology (Specialty Care), US Medical AffairsAbout This RoleThe Medical Director – Immunology (Specialty Care), US Medical Affairs role is a part of Specialty Care, North America (US) Medical, a strategic partner within Biogen, that helps inform medical practice across our therapeutic areas...
-
Scientific Director, Medical Affairs
2 weeks ago
Cambridge, Massachusetts, United States AbbVie Full timeJob SummaryThe Associate Scientific Director, Medical Affairs will provide strategic and operational input into core medical affairs activities, including health care professional and provider interactions, generation of clinical and scientific data, educational initiatives, and safeguarding patient safety.Key ResponsibilitiesContribute to the development of...
Senior Director, Field Medical Affairs
4 months ago
Apnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway muscles to maintain an open airway during sleep. Based in Cambridge, Mass., we are developing a portfolio of novel pharmacologic therapies for sleep apnea and related disorders.
The Senior Director, Field Medical Affairs, will be responsible for building and leading the Medical Science Liaison (MSL) team and overseeing development and execution of the Medical Affairs field strategy in preparation for the launch of Apnimed’s lead compound, AD109. This role will focus heavily on establishing relationships with key external stakeholders, including health care professionals (HCPs) and key opinion leaders (KOLs) while ensuring alignment with organizational objectives. The ideal candidate will be a true medical “triple threat” demonstrating high levels of scientific excellence, business acumen, and emotional intelligence.
This leader will report to the Vice President, Medical Affairs, and may be based remotely.
Key Job Duties include, but are not limited to:
- Recruit, train and manage a high-performing team of U.S. MSLs, fostering a culture of excellence and continuous development
- Provide leadership and support to direct reports, ensuring they have the necessary tools, guidance and training to elevate their business and scientific acumen and execute consistent, high-quality interactions with key stakeholders
- Develop and implement field processes, metrics and strategic territory plans that optimize MSL activities in alignment with medical affairs objectives
- Oversee appropriate scientific exchange with the external medical community, ensuring fair and balanced communication of medical and scientific information, as well as pull-through of key scientific messaging relevant to Apnimed’s pipeline
- Identify and cultivate strong relationships with HCPs, KOLs, digital opinion leaders (DOLs) and payers to drive scientific dialogue relevant to AD109 and raise awareness of the unmet needs in obstructive sleep apnea
- Gather and communicate field insights to drive actionable recommendations to inform medical and commercial strategy.
- Work in close partnership with cross-functional teams, including Medical Affairs, Market Access, Clinical Development and Sales(when they are hired) in a compliant manner to ensure strategic and tactical alignment, enhance communications between headquarters and field functions, and maximize in-field effectiveness
- Build and maintain technical and clinical expertise in obstructive sleep apnea, including awareness of current treatment strategies, market issues and trends, and new therapeutic developments to inform strategy and identify opportunities for growth
- Ensure Field Medical Affairs team adherence to company policies, regulatory guidelines and compliance requirements in all aspects of HCP interactions and scientific exchange.
Education:
- Doctoral degree in life sciences required (MD, PharmD or PhD)
- Training in pulmonary, neuroscience, sleep medicine or other chronic disease area preferred
Work-related Skills & Experience
- 10+ years of biopharmaceutical industry experience as a MSL required, with 5+ years of experience developing and managing a field MSL team
- Demonstrated ability to lead and inspire a team, fostering a collaborative and results-driven environment
- Excellent communicator with exceptional interpersonal skills and the ability to effectively engage with diverse stakeholders
- Experience with all phases of drug development, including multiple drug launches across a variety of therapeutic areas
- Additional experience working in headquarter roles including Clinical Development, Medical Affairs or Market Access preferred
- Proven ability and affinity to work collaboratively in a cross-functional environment
- Keen ability to quickly and consistently build and maintain high levels of trust with internal and external stakeholders
- Strategic mindset with the ability to analyze complex data to inform decision-making and drive operational excellence
- Skilled in interpreting medical literature and translating data into a compelling scientific story
- Highly resourceful, self-motivated and has the ability to thrive in an entrepreneurial environment
- Unimpeached track record of the highest levels of integrity, honesty and ethics
- Ability to travel up to 50%, including overnight stays as needed
What Apnimed Offers:
- 401(k) with company match
- Generous time off for vacation
- Generous healthcare benefits
- Flexible working environment
- Motivated and experienced team
Location and Other Information:
- Apnimed is a privately held company based in Cambridge, MA; we are generally virtual and specific location within the US is flexible.
- Apnimed is an EEO employer committed to an exciting, diverse, and enriching work environment.
- Please visit us at www.apnimed.com to learn more about our work with Obstructive Sleep Apnea
