Director, Compliance
$200k - $270kBioSpace, Inc.
Company Overview Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We develop therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at and follow us on X, LinkedIn and Facebook. Role Summary The Director of Compliance provides compliance guidance on a wide range of commercialization issues as Dyne scales and prepares for the anticipated launch of its first therapies. These topics include HCP and patient engagement, disease-state education, compliance with FDA regulations, health care fraud and abuse laws, Value & Access matters, patient support programs, data privacy, and various federal and state laws governing the pharmaceutical industry. The Director of Compliance helps design and implement a global compliance program to ensure that Dyne complies with all applicable laws, regulations, and ethical codes where the company operates. The Director works closely with Medical, Commercial, Regulatory Affairs, and G&A colleagues. We seek a strategic, collaborative, solutions-oriented leader with deep knowledge and experience. Prior rare-disease and launch experience enables the Director of Compliance to help Dyne navigate the challenges of our first therapy launches. This role is based in Waltham, MA, and is not remote. Primary Responsibilities Design and implement a comprehensive health care compliance program that aligns with laws, regulations, policies, and industry standards. Establish and update corporate policies, procedures, and guidelines to support compliant operations across Commercial, Medical and research activities. Lead risk assessments to identify and prioritize compliance risks. Develop and deliver risk-based compliance training for employees. Develop and implement auditing and monitoring plans and related dashboards. Lead confidential, thorough investigations into potential compliance violations. Establish Compliance as an approachable, knowledgeable, practical, helpful, and solutions-oriented business partner. Collaborate closely with the Franchise Counsel to align on consistent, actionable legal and compliance solutions. Champion Dyne’s core values and culture of integrity. Serve as a trusted advisor to senior leadership and cross-functional teams on business and compliance strategies. Perform additional duties as required. Experience and Skills Advanced degree in law, business administration or a related field. 10+ years of overall professional experience, with at least 7+ years in healthcare compliance, ideally within a global rare disease biotechnology company. Deep expertise in U.S. health care laws, federal health care programs, and therapy launches. Strong understanding of the PhRMA Code, Anti-Kickback Statute, False Claims Act, data privacy, and transparency laws. Experience supporting compliant patient engagement, HCP engagement, scientific exchange, and innovative patient support programs. Proven success advising cross-functional teams (Medical, Commercial, Regulatory, Technical Operations, and G&A) on complex, time-sensitive matters. Skilled at balancing strategic compliance guidance with practical business judgment in fast-paced, evolving environments. Exceptional communication, analytical, and project management skills with attention to detail and execution excellence. Collaborative leadership style and enterprise mindset that reinforces organizational culture and values. Experience thriving in a small, rapidly growing biotech or start-up environment with a solutions-oriented approach. Salary MA Pay Range: $200,000 - $270,000 USD The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload. Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. #J-18808-Ljbffr
$180k - $226.05k
...Relationships, Urgency, Excellence and Innovation – TRUE Innovation ! Position Summary: Zenas BioPharma is looking for a Director of Global Compliance to play a central role in shaping and advancing our global ethics and compliance program as we move toward commercial...SuggestedFull timeWork at officeFlexible hours$191k - $236k
...Overview The Director, Legal and Compliance, serves as a trusted strategic partner and is responsible for providing practical and thoughtful legal counsel to the Commercial, Medical Affairs, Market Access, and Patient Support functions in support of assigned products....Suggested$250k - $273k
The Senior Director, Quality Compliance is responsible for providing strategic leadership and oversight of the organization’s global quality compliance programs, ensuring alignment with regulatory requirements and industry best practices. This role leads key quality systems...SuggestedWork at officeRemote work- ...most. This role is based in our Lexington, MA office and requires employees to be onsite five days per week. Role Senior Director, Healthcare Compliance, reporting to the VP, Head of Compliance, will serve as the primary Compliance & Ethics business partner to the...SuggestedWork at office
$250k - $280k
Responsibilities Define and lead the Compliance & Ethics strategy for Commercial and other key business areas, aligning priorities with growth, product lifecycle, and market expansion. Serve as the accountable Compliance & Ethics business partner for Commercial, Medical...Suggested- ...candidates for well-validated targets.Reporting to the Senior Director, Regulatory Affairs, the Associate Director, Regulatory Affairs... ...development and maintenance of programs while ensuring compliance with applicable regulatory requirementsParticipate in or lead...Temporary workWork at officeLocal areaImmediate start3 days per week
- ...help them achieve their goals.Job DescriptionReporting to the Director of the Office for Community Support, Non-Discrimination, Rights... ...University Title IX Coordinator, the Associate Director for Compliance and Title VI Coordinator is responsible for oversight of the University...Work at officeLocal area
$138.75k - $231.25k
Associate Director Regulatory Affairs, OncologyAt GSK, we have bold ambitions for patients, aiming to positively impact the health of... ...Medicines Profile. This goal has to be achieved while ensuring compliance with both internal GSK process / policy and with appropriate...Full timeLocal area- ...serve as Teledyne’s subject matter expert for Jurisdiction & Classification (JC), driving global consistency and strengthening our compliance posture worldwide. You’ll shape how advanced technologies move across borders, influence product design, ensure global compliance...Minimum wagePermanent employmentFull timeWork experience placementLocal areaWorldwide
$132.6k - $198.9k
...expected to foster connection and teamwork by being present in the office at least 2 days per week. The Opportunity Are you a compliance professional with extensive experience navigating Medicaid, Medicare, and commercial dental regulations? Join Sun Life's U.S....Full timeWork at officeLocal areaFlexible hours2 days per week$270k - $310k
...follow us on X, LinkedIn and Facebook.Role Summary:The Executive Director, Regulatory Affairs serves as a visionary leader who shapes... ...strategic program direction for regulatory affairs, ensuring compliance with applicable regulations and maintaining strong relationships...Local area$116k - $160k
Company DescriptionDeciphera, a member of Ono Pharmaceutical Co., Ltd., is a biopharmaceutical company focused on discovering, developing, and commercializing important new medicines and providing hope to people living with cancer, neurologic and autoimmune disease. Deciphera...Flexible hours- ...created a robust pipeline of differentiated investigational therapeutic candidates for well-validated targets. Reporting to the Senior Director, Regulatory Affairs, the Associate Director, Regulatory Affairs will represent Regulatory Affairs on assigned cross-functional...Work at office3 days per week
- ...preferred 10+ years of professional experience in legal, regulatory, compliance environments; attorneys with “Big Law” and/or in house... ...family.WHAT YOU'LL DOAs the Ethics & Compliance (E&C) Associate Director of Investigations, you will lead in driving and shaping the...Apprenticeship
$171k - $209k
...motivated for change. Just imagine the possibilities of what we can do together. How You Will Achieve More:The Associate Director, Healthcare Compliance, will play a critical role in building and supporting Intellia’s Healthcare Compliance Program in connection with the...Full time$70 - $75 per hour
...within a dynamic biopharma environment. Reporting to the Senior Director of Regulatory Affairs, you will help drive high-quality... ...support regulatory operations, ensuring deliverables meet quality, compliance, and timeline expectations.Contribute to the planning and execution...Contract workTemporary workWork at officeLocal areaMonday to Friday$207k - $253k
## Director, Regulatory Affairs CMCApplylocations: MA - Waltham - Officetime type: Full timeposted on: Posted 3 Days Agojob requisition id: JR\_000763Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis...Minimum wageFull timeLocal areaFlexible hours$207k - $253k
Overview Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction‑associated steatohepatitis (MASH). This role provides strategic, tactical and operational regulatory CMC leadership to support clinical trial applications...Full timeFlexible hours- ...development teams, primarily focused on (but not limited to) drug products.Provide regulatory oversight and guidance to project teams on compliance matters, FDA requirements, clinical study design issues and on timing, logistics and operational recommendations for product...
$145k - $215k
Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD...Full timeFlexible hours- Company DescriptionArtech Information Systems is the #1 Largest Women-Owned IT Staffing Company in the U.S. and an employer of choice for over 7,500 consultants. We recruit world-class talent for IT, engineering, and other professional jobs at 70+ Fortune and Global 500...For contractors
$259k - $317k
...in the lives of patients we serve.Position Summary:The Senior Director of Regulatory Affairs is a senior leader responsible for developing... ...that accelerate product development while ensuring full compliance with applicable regulations and guidance.Responsibilities:Develop...Full timeWork at officeFlexible hours$195k - $330k
...Collaborate with and provide regulatory oversight of CDMOs and other external manufacturing/testing partners to ensure regulatory compliance and submission readiness.Scale and lead the Regulatory Affairs CMC function as the pipeline and organization grow.Skills and...$134k - $149k
...support the development and maintenance of programs, while ensuring compliance with applicable regulatory requirements. The ideal candidate... ...department and across R&D. This role reports to the Executive Director, Head of Orexin Regulatory Strategy.Why join Team Alkermes?...Work at officeLocal areaFlexible hours3 days per week$145k - $215k
...to serve as a key regulatory contributor and emerging strategic leader across multiple drug development programs. Reporting to the Director of Regulatory Affairs, the Senior Manager will independently lead regulatory activities at the study level, acting as the...- ...Role We are seeking a highly skilled and experienced Associate Director / Director of Regulatory Affairs to join our growing clinical... ...overseeing and managing global regulatory activities to ensure compliance with applicable laws, regulations, and guidelines. In this...
$175k - $206.02k
Associate Director / Director, Regulatory Affairs About the Role We are seeking a highly skilled and experienced Associate Director /... ...overseeing and managing global regulatory activities to ensure compliance with applicable laws, regulations, and guidelines. In this...$170k - $230k
Associate Director, Regulatory Affairs CMC Waltham, MA Skyhawk Therapeutics is seeking a hands‑on Associate Director, Regulatory Affairs CMC (RegCMC) to support the development and execution of the global RegCMC strategy for Skyhawk's small molecule pipeline. Working...- Alexion Pharmaceuticals, Inc. is seeking an Associate Director of Advertising and Promotion Compliance in the US to serve as the RA representative for assigned products and therapeutic areas. The role involves reviewing and approving regulatory content for promotion, disease...
$225k - $263k
The Senior Director, Healthcare Compliance Business Partner will be the primary Compliance Business Partner supporting our Commercial, Medical Affairs, Patient Services, and Patient Advocacy functions. This broad position will work to assist in the implementation, maintenance...Work at officeRemote workFlexible hours
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