Senior Director, Compliance
Inventiva Pharma
Inventiva is a clinical-stage biopharmaceutical company headquartered in France, focused on the development of lanifibranor in a Phase 3 trial, NATIV3, in MASH. To learn more, please visit: We are strengthening our compliance infrastructure and seeking a Senior Director, Compliance to lead and scale our global compliance and data privacy programs. The Opportunity Reporting to the Chief Legal Officer , the Senior Director, Compliance plays a critical leadership role in ensuring the company meets its legal, regulatory, and ethical obligations globally. This individual will lead the continued development, implementation, and oversight of comprehensive healthcare compliance and data privacy programs, while partnering extensively across the organization during a pivotal stage of growth. This is a highly visible role that will support late‑stage clinical operations today and help establish the foundation for post‑readout readiness and future commercialization. Key Responsibilities Compliance Program Leadership Lead the design, implementation, and continuous improvement of global healthcare compliance programs aligned with evolving laws, regulations, and industry codes Partner cross‑functionally to support adherence to healthcare compliance requirements and ethical standards Develop, maintain, and update compliance policies, procedures, and processes to meet global requirements Training, Systems & Oversight Develop and deliver compliance training programs that promote understanding of and adherence to company policies Implement and manage compliance systems and tools (e.g., HCP engagement, analytics, monitoring platforms) Support enterprise‑wide compliance risk assessments and contribute to the annual compliance workplan Data Privacy & Transparency Partner with the Data Protection Officer (DPO), Legal, and IT to support a comprehensive global data privacy program aligned with HIPAA, GDPR, CCPA/CPRA, and other applicable regulations Assist in conducting Data Protection Impact Assessments (DPIAs) and privacy risk assessments across clinical trials and third‑party vendor relationships Implement systems and procedures to ensure compliance with global transparency and spend reporting requirements Partner cross‑functionally to establish procedures for the development, review, and approval of publications and promotional materials Lead the Medical, Legal, and Regulatory (MLR) review committee Monitoring, Investigations & Culture Conduct and support monitoring and auditing activities to assess program effectiveness and identify compliance risks Lead and support internal compliance investigations through resolution and reporting to leadership Administer compliance reporting channels (e.g., helpline) and promote a strong speak‑up culture across the organization Proactively identify inefficiencies within compliance and privacy programs and implement enhancements Qualifications Degree in Law or a related field required Minimum of 10 years of healthcare compliance experience, preferably within biotech or pharmaceutical organizations Strong working knowledge of global healthcare regulations, compliance frameworks, and industry codes Demonstrated experience supporting late‑stage clinical development and readiness for commercialization Core Skills & Competencies Healthcare compliance and ethics Risk assessment, monitoring, and auditing Investigations and issue management Policy development and governance Data privacy and regulatory interpretation Strong analytical, communication, and project management skills Ability to manage multiple priorities in a fast‑paced, evolving environment Why Join Us Join the company at a transformational moment Work closely with experienced executive leadership during a critical growth phase Opportunity to shape scalable compliance and privacy programs for a potential commercial organization All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law. #J-18808-Ljbffr Inventiva Pharma
- ...Senior Director, IT Compliance & Governance (Contractor) About the Company Innovative company designing & developing gene therapeutic products Industry Biotechnology Type Public Company Founded 2013 Employees 51-200 Categories Biotechnology...SeniorFor contractors
- Harvard University Central Administration seeks a Senior Director for the Harvard International Office. You will set the vision for international... ...students, scholars, and staff, ensuring regulatory compliance and a resilient service portfolio across the university. You...SeniorWork at office
$251.77k - $307.72k
...imagine the possibilities of what we can do together. How You Will Achieve More:We are seeking an experienced QMS and Digital Compliance Senior Director to lead transformational change within our quality compliance organization. This leadership role is responsible for...SeniorFull time- Manulife seeks an experienced Financial Crime Compliance leader to oversee regulatory obligations and risk across its US insurance, wealth, and asset management businesses. You will advise senior leaders, engage regulators, and play a key role in advancing the modernization...Senior
- Manulife Financial is seeking an experienced Financial Crime Compliance leader to serve as the senior representative for the United States businesses. This role oversees AML, sanctions, fraud, anti-bribery and corruption, and broader Financial Crime compliance across Insurance...Senior
- Northeastern University is seeking a Director of Graduate Financial Aid to lead all aspects of financial aid, including application and... ...This role manages the graduate financial aid team and ensures compliance with policies while providing top-notch counseling to students...Senior
- The Senior Director of the Harvard International Office at Harvard University provides strategic, operational, and financial leadership for the HIO. You will set the vision, ensure compliance with federal and institutional policies, and build a robust service portfolio...SeniorWork at office
- ...Summary Description: The Reg Nonclinical / Clinical Associate Director will lead, conceive, communicate and execute upon the global clinical... ...AD will typically collaborate, influence and negotiate with senior Nonclinical / Clinical leaders on product strategies and...Senior
$145k - $215k
...heard.How you’ll make an impact:Kymera Therapeutics is seeking a Senior Manager, Regulatory Affairs to serve as a key regulatory... ...leader across multiple drug development programs. Reporting to the Director of Regulatory Affairs, the Senior Manager will independently lead...Senior$172.5k - $222.5k
...stakeholder.What you’ll be responsible for: Circle is looking for a Senior Manager to join the Regulatory Assurance team who will help to... ...central global function focused on developing a best in class compliance management system, supporting all regional and core compliance...SeniorFlexible hours- Harvard University’s Central Administration seeks a Senior Director for the Harvard International Office (HIO) to provide strategic, operational... ...leads a diverse team, ensures federal and institutional compliance, and partners with schools, departments, and external...SeniorWork at office
- SBM Management Services, LP in Boston, MA seeks an EHS Director to provide comprehensive environmental, health and safety leadership... ...implementation and administration of SBM's EHS program, ensuring compliance with OSHA and other regulations while fostering a culture of...Senior
$137k - $215.27k
...regulations and guidelines and can apply this understanding to projects to enhance probability of regulatory success and regulatory compliance.Ability to draw from precedents and other regulatory intelligence beyond regulations. Strong analytical or process understanding...SeniorMinimum wageTemporary workLocal areaRemote workWorldwide- ...requirements • Develop and implement procedures, policies, and systems to support commercial and clinical stage operations • Drive compliance with current regulations and oversight of external GMP Quality operations at partner and CMO sites • Help define and drive the...SeniorFlexible hours
$275k - $315k
...OverviewBicara Therapeutics is seeking a strategic and experienced Senior Director of Regulatory Affairs to lead and execute US regulatory... ..., efficient execution of global regulatory plans.Ensure compliance with applicable global regulations and internal quality and...SeniorFull timeTemporary workWork at officeLocal area3 days per week- ...Senior Regulatory Affairs Manager- REMOTE I'm looking for a senior manager, regulatory affairs to lead our growing, dynamic team... .../health authorities Monitor regulatory timelines and ensure compliance with all applicable regulations for IND maintenance Lead in...SeniorFull timeRemote work
$168.75k - $257.8k
...America. Catalent Pharma Solutions in Chelsea, MA is hiring a Director of Quality who will provides leadership and daily management... ...to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee...SeniorContract workLocal area- FTI Consulting is seeking a senior accounting professional to manage monthly accounting packages, financial statement preparation under... ...oversee staff, interact with clients, and support audits, tax compliance and special accounting projects, including IPO-related work,...Senior
- ...professional experience in legal, regulatory, compliance environments; attorneys with “Big Law”... ...trust-based relationships with senior leaders within and outside of the team;... ...managing concerns.Your role reports to the Director of Ethics in Allegations Management.SeniorApprenticeshipWork at office
$196.7k - $353.4k
The RoleModerna is seeking an individual to lead development and execution of global regulatory strategy for programs in its oncology portfolio. This leader will shape regulatory pathways for novel, first-in-class therapeutics and drive successful global development and...SeniorPermanent employmentFull timeWork at officeWork from home- Genetix Biotherapeutics is seeking a Sr. Director, Regulatory Affairs in Boston to lead regulatory activities for product labeling and U.S. advertising compliance. The candidate will ensure that all materials are compliant, meet scientific standards, and align with corporate...SeniorFull time
$218.06k - $327.09k
Job Title: Senior Director, Regulatory Affairs Strategy - Cell Therapy Available locations: Gaithersburg, MDBoston, MASouth San Francisco... ...: Maintain accountability for product maintenance and compliance activities associated with marketed brands, ensuring continued...SeniorHourly payFull timeTemporary workStart working todayWork at officeFlexible hours3 days per week$232k - $348k
Job DescriptionThe Regulatory Strategy Senior Director is a regulatory leader with expert technical and tactical experience in regulatory strategy for the assigned global or regional position and will be responsible for overseeing the development and implementation of advanced...SeniorFull timeSummer workWork at officeLocal areaRemote workFlexible hours2 days per week3 days per week- Boston, MAOpen to RemoteFull Time$150k - $170kJob Description An established organization is seeking a Senior Compliance Manager to support and drive compliance initiatives across regulated environments. This role focuses on ensuring processes, systems, and operations align...SeniorFlexible hours
- ...lead regulatory strategies for Class II medical devices. Responsibilities include managing FDA submissions, ensuring regulatory compliance throughout product development, and collaborating with cross-functional teams. The ideal candidate has over 7 years of experience...Senior
- Title: Director / Senior Director, Global Regulatory Lead Location: San Francisco, CA or Boston, MA -> hybrid 3-days per week (relocation offered!) Overview A growing oncology biotech is seeking a Director / Senior Director, Global Regulatory Lead to drive global regulatory...SeniorRelocation3 days per week
- Senior Manager - Regulatory Affairs Operations Location - Cambridge, MA (Hybrid) Oncology Biotech | Global Clinical Programs I’m currently... ...global regulatory submissions. The Role Reporting into the Director of Regulatory Affairs Operations, you will provide hands‑on...Senior
$212k - $333.19k
...Our goal is to accelerate access to transformative medicines and make a lasting impact on patients worldwide.Join Takeda as a Senior Director, Global Regulatory Lead - Oncology, where you will be part of the global regulatory team. In this influential role, you will lead...SeniorMinimum wageTemporary workLocal areaRemote workWorldwide$242k - $313.5k
...immune‑mediated diseases can live life fully. Job Summary The Senior Director, Regulatory Affairs CMC - Biologics provides senior‑level... ...tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are...SeniorLocal areaFlexible hours2 days per week- ...part of pharma's digital transformation is adherence to industry-accepted standards like GxP, ISO 9001, and 21 CFR Part 11. As Senior Compliance Manager, US, you will operate as an independent senior IC — accountable for ensuring TetraScience's products and platform meet...SeniorImmediate startFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Director, Compliance. Be the first to apply!
- regulatory cmc manager Boston, MA
- regulatory operations manager Boston, MA
- regulatory manager Boston, MA
- director global regulatory affairs Boston, MA
- operations compliance manager Boston, MA
- manager regulatory affairs Boston, MA
- head compliance Boston, MA
- compliance manager Boston, MA
- compliance director Boston, MA
- senior director regulatory affairs Boston, MA

