Director, Clinical Research & Regulatory Affairs
$230k - $245kButterfly Network
Director of Clinical Research Company Description Butterfly Network, Inc. (NYSE: BFLY) is driving a digital revolution in ultrasound imaging and sensing with its proprietary Ultrasound-on-Chip™ semiconductor technology and software solutions. Butterfly first proved its technology in the point-of-care ultrasound market – commercializing the world’s first single-probe, whole-body portable ultrasound device, which is now on its best-selling, third-generation: Butterfly iQ3™. The Company combines its advanced hardware with cloud software and AI, an enterprise workflow solution (Compass AI™) and other offerings to drive adoption of affordable, accessible ultrasound. Butterfly also enables third-party development of imaging AI apps through Butterfly Garden™, its software development kit and AI partnership initiative. In addition to its medical imaging products, Butterfly Embedded™ is the Company’s Ultrasound-on-Chip™ licensing and co-development program designed to enable a new wave of ultrasound-enabled technologies across non-competitive healthcare markets and beyond. Through Butterfly Embedded™, partners can build and scale novel ultrasound applications powered by Butterfly’s proprietary semiconductor chip and software platform. Butterfly’s innovations have been recognized by Prix Galien USA, Fierce 50, TIME’s Best Inventions and Fast Company’s World Changing Ideas, among other achievements. We’re a team of bold thinkers, problem-solvers, and innovators ready to shape the future of medical imaging. Let’s build something extraordinary together! Job Description The Director of Clinical Research is responsible for leading and managing all aspects of clinical study activities at Butterfly Network. This role requires strategic planning and cross-functional collaboration to generate the clinical evidence needed to support product development and commercial growth. This position reports to the Chief Medical Officer and interacts with senior leadership, KOLs, clinical researchers, and partners. Key Responsibilities Clinical Study Management Lead all company-sponsored clinical studies in compliance with Good Clinical Practice (GCP), including developing Monitoring Plans and Data Management Plans. Design clinical study protocols and statistical plans in collaboration with cross-functional teams. Review and analyze clinical and scientific data to support pre-market and post-market product performance. Develop, revise, and implement SOPs for clinical trials and related activities. I nvestigator Initiated Trials (IIT) Program Manage all aspects of the IIT program, including proposal assessment, research agreements, material shipment, and ongoing collaborator check-ins. Work with the Clinical Research Committee to evaluate and select proposals. Partner with Legal and Finance to develop research contracts and budgets. KOL & External Partnerships Recruit clinicians, KOLs, and research partners for new and ongoing clinical studies. Serve as Butterfly Network's Clinical Science Liaison, providing scientific support and answering research-related questions from external collaborators. Team & Operations Leadership Manage and mentor clinical team members and consultants. Identify staffing and budget needs and delegate priorities effectively. Collaborate with R&D, Marketing, and other cross-functional leaders to align clinical programs with business goals. Qualifications Required: BS degree in Engineering or a Technical Field; advanced degree (PhD, MD, or equivalent) strongly preferred. 7-10 years of experience in the medical device or healthcare industry, with at least 6 years in clinical affairs or clinical trial management. Established network of KOLs and clinical research collaborators. Strong knowledge of GCP, IRB/Ethics Committee requirements, and clinical study design including statistical methodology. Experience writing SOPs and clinical research documentation. Excellent communication, leadership, and cross-functional collaboration skills. Preferred: Experience with AI/ML or Software as a Medical Device (SaMD). Familiarity with ultrasound imaging. Experience with regulatory authority audits. All regulatory affairs responsibilities have been removed. The reporting line now reflects the CMO directly. Values Patient-Centric Innovators: Our mission is THE mission. Empowered to Impact: Every voice matters. One Team, One Goal: Unity fuels progress. Growth Champions: We embrace challenges. Action-Oriented Achievers: We follow through, every time. Location Butterfly offers a hybrid work model for most positions, with team members spending two or more days a week in the office. While flexibility is key, we value in-person connections that spark creativity and teamwork. Our offices are designed for collaboration, with comfortable workspaces, stocked kitchens, and opportunities to connect with peers. This is a hybrid position that can be based in the San Francisco Bay Area or New York City, NY Benefits and Perks Comprehensive health insurance, encompassing dental and vision coverage, is provided to all our employees. As a health-tech company, we prioritize the well‑being of our teams. We also contribute to Health Savings Account (HSA) accounts for all enrolled employees on an annual basis. Comprehensive Employee Assistance Program - we provide access to tools and resources to support your emotional health and day‑to‑day needs. 401k plan and match - we facilitate your retirement goals. Eligible employees will have the opportunity to participate in Employee Stock Purchase Plan (ESPP) Unlimited Paid Time Off + 10 Holiday Days a Year - recharge and come back ready to make an impact Parental Leave - we aim to provide our employees with time to bond with their growing family, along with additional support for primary caregivers to help transition back to work Competitive salaried compensation - we value our employees and show it Equity - we want every employee to be a stakeholder The opportunity to build a revolutionary healthcare product and save millions of lives! Compensation Our estimated salary for this role is between $230,000 - $245,000 + bonus + equity + benefits. Actual pay is determined by multiple factors such as skills, qualifications, experience and market demand. For this role, we are only considering candidates who are legally authorized to work in the United States and who do not now or in the future require sponsorship for employment visa status. Butterfly Network is an E-Verify Company. Butterfly Network is an equal opportunity employer. Regardless of race, traits associated with race, color, ancestry, religion, gender, national origin, sexual orientation, age, citizenship, marital status, disability or Veteran status. All your information will be kept confidential according to EEO guidelines. #J-18808-Ljbffr Butterfly Network
$230k - $245k
Director of Clinical Research Job Description The Director of Clinical Research is responsible for managing and advancing Butterfly Network's clinical... .... 5-7 years of experience in clinical research, clinical affairs, or a related field within medical devices or healthcare....SuggestedContract workWork at office- ...a trusted partner to Sponsors, CROs, and Sites across the research and clinical trials landscape. By blending deep subject matter expertise... ...Expertise in study start‑up optimization, IRB processes, and regulatory compliance. Experience with CTMS platforms (e.g., OnCore)...SuggestedFull timeTemporary workFlexible hours2 days per week3 days per week
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...health, one step at a time. Job Overview The Senior Director, Clinical & Translational Research leads Omada's efforts to demonstrate the clinical value... ..., consultants, and partners. Ensure compliance with regulatory requirements, ethical standards, and industry best practices...Local areaRemote workWork from homeFlexible hours- Overview The Director Clinical Research is a vital role responsible for strategic oversight of registries, sub‑studies, as well as IDE and post... ...will lead a multidisciplinary team to ensure compliance with regulatory requirements, align with corporate objectives, and...Contract workRemote work
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A leading health care system in New York is seeking a Medical Laboratory Director to oversee clinical operations and participate in teaching and research. Ideal candidates will have M.D. or M.D./Ph.D. degrees, be board certified, and possess significant laboratory management...$146k - $277k
...medical oversight of assigned clinical studies in the duty as a... ...Scientist staff and Medical Director colleagues to review clinical... ...input to clinical development or regulatory teams within the Company, upon... ...specific therapeutic area. Clinical research experience required....Contract workWork at officeWorldwideFlexible hours- Butterfly Network is seeking a Director of Clinical Research to lead and manage all clinical study activities. This role requires strategic planning... ...ideal candidate will have a strong background in clinical affairs, proven leadership skills, and an established network in...
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...Manufacturing Co in Pennsylvania is seeking a Director for Personnel Relations at the Abramson... ...Center. The role involves directing research teams to accomplish specific goals and... ...critical operations, including managing clinical research personnel and budgets. Ideal candidates...- Ascension St Vincent is looking for a Director of Pediatric Hospital Medicine at Staten Island University... ...Hospital Medicine and the ability to develop clinical protocols, supervise residents, and engage in clinical research. Along with a competitive salary and extensive...Full time
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Senior Manager, Strategic Partnerships (Clinical Research) General Information Location: Remote Organization: Avoca Job Type: Full Time - Regular Description and Requirements ABOUT WCG WCG’s clinical solutions are built on a foundation of best-in-class clinical services...Full timeContract workWork at officeLocal areaRemote workFlexible hours$84k - $105k
## Program Manager Clinical ResearchApplylocations: 111 East 210th Streettime... ....00-$105,000.00The **Clinical Research Program Manager,** under the supervision of the Director of Quality Assurance, will... ...reviews, pharmacy reviews, regulatory reviews for Montefiore...Work experience placementWork at officeShift work$90k - $120k
Business Development Manager (Clinical Research) Apply to the Business Development Manager (Clinical Research) role at Arizona Liver Health... ...leading clinical trials, ensuring patient safety and regulatory compliance, and generating high-quality clinical data. Our network...Full timeContract workTemporary workWork at officeRemote work- Dormont Manufacturing Co is seeking a Manager for Clinical Research Finance Operations. The successful candidate will be responsible for the overall financial management of clinical research projects, including budget development, compliance, and financial analyses. Located...
- ...Job Description Job Description Manager-Director, Business Development - Clinical Research Manager-Director, Clinical Business Development Full Time Remote-USA Based (Preferably East Coast) Reports to: Senior Vice President, Clinical Services Frontage...Full timeContract workWork at officeRemote workFlexible hours
- Montefiore New Rochelle is looking for a Program Manager Clinical Research to oversee compliance and quality assurance within the Cancer Clinical Trials Office. This role involves managing clinical research monitoring activities and providing constant feedback on compliance...Work at office
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...administrative management of a high-volume clinical trials portfolio. This role is... ...of cardiovascular and vascular clinical research studies and supervising research staff to... ...compliance with institutional, sponsor, and regulatory requirements. Working closely with principal...H1bLocal areaWork visa$105k - $120k
...Annual Bonus Job Overview We are looking to add an experienced Clinical Research Manager to a growing national organization. This position is... ...and in the field environment. Collaborates with the Director of Clinical Research and Director of Quality, Clinical Research...Full timeContract workWork experience placementLive inLocal areaRemote work- A leading medical institution in New York is seeking a Clinical Trials and Regulatory Affairs Manager to oversee regulatory activities for psychedelic-assisted psychotherapy clinical trials. The role requires strong communication and project management skills, along with...
- ...Associate Director, Health Economics & Outcomes Research Secura Bio was established in 2019 with... ...of oncology’s largest clinical and market opportunities... ...Research to join our Medical Affairs organization. The ideal... ..., Market Access, and Regulatory colleagues to ensure integrated...Full time
$130k - $150k
...compensation at the time of posting. Position Summary The Clinical Research Manager (CRM) oversees operational management of clinical research... ...multiple trials, and collaborates with investigators, regulatory teams, research pharmacy, and clinical departments to ensure...Temporary workWork at officeLocal area- **Job title:** Clinical Research Director - Rare Diseases**Location:** Cambridge, MA / Morristown, NJ**About the Job**Join the engine of Sanofi... ..., such as clinical operations, translational medicine, regulatory affairs, biostatistics, drug discovery, drug safety, marketing*...
- A leading recruitment agency is seeking Medical Directors for Oncology Clinical Research roles. Responsibilities include designing and conducting clinical trials, as well as analyzing data. Ideal candidates should possess an M.D. or Ph.D. with extensive drug development...
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Overview The Research Medical Director is a key member of the Clinical and Policy research development area at Cotiviti. The Research Medical Director is responsible for providing leadership guidance to the clinical teams and ensuring the Rules and policies are accurately...Full timeWork at officeImmediate startRemote work$206.25k - $343.75k
## Clinical Research Director - Immunology and InflammationApplylocations: Cambridge, MA: Morristown, NJtime type: Full timeposted on: Posted Todaytime... ..., labeling, and contributes/supports interactions with regulatory agencies and ethics committees. The role requires a self-...Remote work$130k - $150k
Columbia University Irving Medical Center is seeking a Clinical Research Manager to oversee operational management of clinical research studies... ...involves coordinating complex clinical trials, ensuring regulatory compliance, and managing study operations across multiple...
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