Executive Director, Clinical Development

Location: Bridgewater
Posted on: June 23, 2025

Job Description:

Company Description Insmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases. Our most valuable resource is our employees, and everything we do is motivated by a patients-first mentality. We are dedicated to growing our team with talented individuals from around the world who are willing to challenge the status quo, solve problems, and work collaboratively with a sense of urgency and compassion. Guided by our core values of collaboration, accountability, passion, respect, and integrity, we aim to foster an inclusive, diverse, and flexible work environment, where our employees are recognized for leaning in and rolling up their sleeves. If you share our vision and want to work with the most dedicated people in the biopharma industry, come to Insmed to accelerate your career. Recognitions Consistently Ranked Science 's Top Employer Insmed is dedicated to creating a collaborative environment where our team can thrive. Every day, our employees turn their passion for science and research into innovative solutions for patients. That's why we've been named the No. 1 company to work for in the biopharma industry in Science 's Top Employers survey for four years in a row. A Certified Great Place to Work® We believe our company is truly special, and our employees agree. In July 2024, we became Great Place to Work-certified in the U.S. for the fourth year in a row. We are also honored to have been listed on the Best Workplaces in Biopharma™, Best Workplaces in New York™, PEOPLE® Companies That Care, Best Workplaces for Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists. Overview The role will be responsible for the oversight of the strategic clinical development plans and successful conduct and execution of the TPIP clinical development program in pulmonary hypertension-related indications in mid-to-late stage development. In addition, this role will be responsible for strategic direction of clinical aspects of engagements with health authorities related to registration programs and filings. The individual will articulate the project goals, strategy and the underlying science and clinical need to internal and external audiences with clarity and credibility. Responsibilities Leads clinical development teams responsible for mid-to-late stage development of TPIP. Leads the Clinical Program Team (CPT) to effectively make decisions and handle conflict and change. Responsible for maintaining a high degree of CPT effectiveness through collaboration, influence, and, as necessary, coaching and mentoring of cross-functional team members. Representative to matrix Global Asset Team to ensure clinical program is represented and integrated into Global plans across functions. Build strategic and coordinated clinical development plans which are aligned with business objectives and are differentiated from competitor products. Leads and communicates the clinical development strategy at governance meetings, accountable for aligning with internal management and for communicating with external collaborators. Responsible for all clinical aspects of project strategy. Accountable for the delivery of projects partnering with other global development and related functions. Requirements and Qualifications: MD/DO equivalent with preference for Cardiology or Pulmonary formal training. Will consider industry experiences in Pulmonary or Cardiology in drug development. 10 years in biotech of pharma with most in a global clinical development role. Combination drug/device development experience is a plus. Experience with filing original NDA or BLA required with additional sNDA or sBLA experience strongly preferred. Experience with J-NDA a plus. Prefer experience in FDA advisory committee, or CHMP Scientific Advisory Group, or CHMP Oral Explanation experiences. Previous direct people management experience required. Experience working in matrix global development team, e.g. GPT, required. LI-MM1 Salary Range $320,000 - $384,667 a year Compensation & Benefits At Insmed, we're committed to investing in every team member's total well-being, now and in the future. Our benefit programs vary by country but we offer the following to all Insmed team members, regardless of geographic location: Flexible approach to how we work Health benefits and time-off plans Competitive compensation package, including bonus Equity Awards (Long-Term Incentives) Employee Stock Purchase Plan (ESPP) For more information on U.S. benefits click here. Additional Information Insmed Incorporated is an Equal Opportunity employer. We do not discriminate in hiring on the basis of physical or mental disability, protected veteran status, or any other characteristic protected by federal, state, or local law. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. Unsolicited resumes from agencies should not be forwarded to Insmed. Insmed will not be responsible for any fees arising from the use of resumes through this source. Insmed will only pay a fee to agencies if a formal agreement between Insmed and the agency has been established. The Human Resources department is responsible for all recruitment activities; please contact us directly to be considered for a formal agreement. Insmed is committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. To request reasonable accommodation to participate in the job application or interview process, please contact us by email at TotalRewards@insmed.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. Applications are accepted for 5 calendar days from the date posted or until the position is filled.

Keywords: , East Brunswick , Executive Director, Clinical Development, Science, Research & Development , Bridgewater, New Jersey