Director of Compliance

Join Iterative Health as our Director of Compliance, where you will play a pivotal role in shaping our compliance strategy and ensuring adherence to regulatory requirements. This leadership position will involve developing and implementing compliance programs, monitoring compliance performance, and liaising with regulatory bodies. You will lead a team of compliance professionals and collaborate with various departments to cultivate a culture of compliance within the organization.

The Associate Director for Compliance and Title VI Coordinator plays a pivotal role in ensuring the University adheres to Title VI regulations and oversees the management of Title IX Hearings, Appellate Panels, NDAB Determination Panels, and cases under the University Committee on Rights and Responsibilities (UCRR) Fact-Finding Procedures. Reporting to the Director of the Office for Community Support, Non-Discrimination, Rights and Responsibilities (CSNDR) and the University Title IX Coordinator, this position collaborates closely with various stakeholders including the Title IX Hearing Chair and the Director of the Office for Dispute Resolution (ODR). The Associate Director provides leadership in the administration of UCRR Fact-Finding Procedures, working in conjunction with the University President and Faculty Panels. Key Responsibilities: Offer guidance and support to Hearing, Appellate, and Determination Panels, as well as local Title IX Resource Coordinators and personal advisors regarding applicable Policies and Procedures.Facilitate logistical arrangements for the University President or their designee, along with UCRR Faculty Panels.Oversee the intake process for all complaints filed under the NDAB, particularly those alleging discrimination based on Title VI protected characteristics.Prepare essential materials including summaries and notices for Hearing, Determination, and Appellate Panels.Lead the development of the Annual Report published by the Director of CSNDR, detailing complaints under the NDAB.Act as the primary liaison for communications and materials pertaining to various panels and stakeholders.Create and implement internal guidance and training resources for Hearing and Appellate Panels.

Amylyx Pharmaceuticals is dedicated to revolutionizing the treatment of diseases with significant unmet needs. We embrace challenges as opportunities, driven by a sense of urgency, rigorous scientific methodology, and a steadfast commitment to the communities we serve. Our focus is on clinical-stage development for conditions such as post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).Our mission thrives on our talented team, which embodies core values of audacity, curiosity, authenticity, engagement, and accountability — all of which foster a culture of care. Amylyx has curated a skilled workforce ready to act swiftly because the communities we support cannot afford to wait. If you are passionate about addressing some of the most challenging issues in medicine, we invite you to explore the opportunity below and apply.The OpportunityThe Associate Director of Computer System Validation (CSV) & Quality Compliance will provide enterprise-level leadership, strategic direction, and governance for the validation, lifecycle management, and continuous compliance of GxP-relevant computerized systems, particularly focusing on the Veeva Quality Suite. This position is pivotal in ensuring that our digital quality solutions and supporting systems comply with global regulatory standards (FDA, EMA, ICH, GAMP 5), safeguard data integrity, and maintain a sustainable, inspection-ready status across the organization.This role entails close collaboration with Quality, IT, Regulatory, Clinical, and business process owners to define system requirements, oversee new system implementations and significant enhancements, and promote harmonized, risk-based validation practices. Additionally, this position supervises quality compliance processes such as Change Control, Deviations, CAPA, and continuous improvement, ensuring timely resolutions, trend analysis, and effective governance through leadership of key forums, including Quality Management Review and cross-functional compliance meetings.

We are seeking a dedicated and detail-oriented Compliance Officer to join our dynamic team at ttp1 in Cambridge. As a Compliance Officer, you will play a crucial role in ensuring that our operations comply with regulatory requirements and internal policies. You will be responsible for conducting compliance audits, monitoring adherence to regulations, and implementing compliance training programs.The ideal candidate will possess strong analytical skills, attention to detail, and the ability to communicate compliance matters effectively across all levels of the organization. Join us in our mission to uphold the highest standards of compliance and integrity.

The Compliance Specialist at Harvard University supports the financial administration team by monitoring activities to ensure alignment with applicable laws and regulations. This position is based in Cambridge and centers on upholding standards that protect the university’s financial integrity. Key responsibilities Track and review compliance activities related to financial operations Conduct audits to identify and address areas of risk Help implement policies designed to prevent noncompliance Skills and qualities Strong analytical skills to assess processes and spot discrepancies Attention to detail when reviewing records and procedures Commitment to maintaining high standards in financial administration

At Raspberry Pi, we take pride in creating an inspiring environment where our team can excel at what they love. By joining us, you will become part of a dedicated group committed to democratizing technology and providing affordable computing tools to people all around the world. We are currently in search of a meticulous and experienced Trade and Compliance Lawyer to enhance our dynamic legal team. In this role, you will play a crucial part in guiding our international trade compliance and sanctions efforts, along with addressing various regulatory and compliance challenges faced by a leading global technology firm. We seek candidates with a minimum of 8 years of post-qualification experience, ideally with a background in-house at a UK-listed technology company (though this is not a strict requirement). You should possess a collaborative spirit and excellent communication skills, as you will be closely interacting with our commercial and finance teams. A pragmatic, risk-aware approach to legal and commercial decision-making is essential. This position is full-time and reports directly to the General Counsel at our office located on the Science Park in Cambridge. We are open to considering part-time and remote work arrangements. As a subject matter expert, you will provide advisory services on sanctions and export controls, licensing risks, and compliance with various global sanctions regimes including those imposed by the UK, EU, UN, and the US, as well as our internal policies. Ideally, you will possess broader expertise in areas such as intellectual property, competition law, GDPR, and anti-bribery and corruption, along with managing governance policy frameworks. Your responsibilities will include advising on risk management decisions concerning suppliers, customers, and transactions that may have sanctions and regulatory compliance implications; delivering expert advice and training; assessing appropriate risk controls; and overseeing regulatory reporting processes related to sanctions and other compliance concerns within the organization.

As a Governance, Risk, and Compliance (GRC) Analyst at Gearset, you will play a crucial role in ensuring that our operations align with industry standards and regulations. You will be responsible for conducting risk assessments, implementing compliance frameworks, and collaborating with cross-functional teams to promote a culture of compliance throughout the organization.This is an exciting opportunity to contribute to the integrity and security of our systems while working in a dynamic and innovative environment.

Join Steritech as a Food Safety and Compliance SpecialistLocation: Cambridge, OntarioSteritech is a leader in food safety and quality assurance, serving as a trusted partner to some of the most recognized brands across various sectors including manufacturing, food service, retail, and hospitality. Our mission is to empower clients to deliver the safest and healthiest experiences to their customers. As part of the Rentokil Terminix family, we uphold the highest standards in food safety and compliance.Your Future Starts Here! At Steritech, we are dedicated to fostering a culture of continuous learning and professional growth. With a majority of our management team having advanced from specialist roles, we believe in nurturing talent from within. Joining our team means embarking on a career path filled with opportunities for advancement. We equip you with the necessary tools, resources, and mentorship to ensure your success, as we recognize that your achievements contribute to our collective success.As a Food Safety & Compliance Specialist, you will partner with clients in the hotel, restaurant, and grocery sectors to ensure adherence to brand standards, food quality, and exceptional service.Key Responsibilities:Conduct thorough assessments to evaluate compliance with regulatory, industry, and proprietary standards.Monitor food preparation and cooking practices to uphold food safety and sanitation standards.Collaborate with clients to identify and address the root causes of discrepancies in assessments while developing corrective action plans.Educate and guide clients on creating a safer and healthier workplace for their employees and customers.Willingness to travel up to 50% of the time by car and/or plane, approximately 10 overnight stays per month.

Scholar Rock is a pioneering biopharmaceutical company dedicated to discovering, developing, and delivering transformative therapies for patients with serious diseases that exhibit significant unmet needs. Renowned globally for our expertise in the biology of the transforming growth factor beta (TGFβ) superfamily, we are committed to advancing innovative treatments where protein growth factors are critical. Over the last decade, we have built a robust pipeline that has the potential to redefine the standard of care for neuromuscular diseases, cardiometabolic disorders, cancer, and various other conditions where growth factor-targeted therapies can make a significant impact.Scholar Rock uniquely demonstrated clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). Our dedication to exploring fundamentally different therapeutic avenues is driven by the innovative application of our proprietary platform, which has produced novel monoclonal antibodies that modulate protein growth factors with remarkable precision. By leveraging cutting-edge scientific research in disease areas historically underserved by conventional treatments, we work tirelessly to create new opportunities for patients. Discover more about our approach at ScholarRock.com and follow us on @ScholarRock and on LinkedIn.Position Overview:The Director or Senior Director of Regulatory Strategy, reporting directly to the Senior Vice President, Global Head of Regulatory Affairs, will be responsible for formulating and executing the global regulatory strategy for designated clinical and pipeline programs. As a subject matter expert, this individual will engage with program teams to identify regulatory risks and opportunities, thereby informing strategic direction and planning. The ideal candidate will spearhead interactions with regulatory authorities, overseeing the preparation and submission of all regulatory documentation and correspondence.

We are seeking a dedicated and knowledgeable Senior Associate in Operational Excellence & Compliance to join our dynamic team at Integrated Resources Inc. In this pivotal role, you will contribute to enhancing our operational processes and ensuring compliance with industry regulations. You will collaborate with cross-functional teams to identify opportunities for improvement and implement best practices that drive operational efficiency.

Join Flagship Pioneering Inc. as the Director/Senior Director of Compensation, where you will lead the strategic development and execution of our compensation programs. Your role will involve designing competitive compensation structures, ensuring alignment with industry standards, and driving initiatives that enhance employee engagement and performance. You will collaborate with senior leadership to shape compensation policies that reflect our commitment to attracting and retaining top talent.

Join Luminance, the trailblazer in Legal-Grade™ AI for enterprises. With backing from prestigious VCs and recognition on both Forbes AI 50 and Inc. 5000 listings, we are revolutionizing the legal sector worldwide.We are looking for a proactive Compliance Analyst to enhance and manage our information security compliance programs, focusing on ISO/IEC 27001:2022, SOC 2 (Type I & II), and CMMC Level 1.This key role will ensure that our compliance processes are robust, scalable, and in sync with our growth strategy. The successful candidate will collaborate with Security, Procurement, Legal, and Engineering teams to implement effective compliance practices across the organization.

As a Governance, Risk, and Compliance (GRC) Manager at Gearset, you will play a pivotal role in ensuring that our operations align with regulatory requirements and internal policies. You will lead the strategic development of our GRC framework, manage compliance audits, and champion risk management practices across the organization.Your expertise will help us navigate complex regulatory landscapes while promoting a culture of accountability and transparency. Join us in safeguarding our reputation and fostering a compliant environment that drives our business forward.

Your Role at Lila Sciences Lila Sciences is seeking a proactive and strategic Director of Facilities to oversee the daily operations and long-term management of our diverse facilities. You will be responsible for developing a scalable facilities strategy, ensuring safety and compliance across all sites, and managing budgets, capital planning, vendor relationships, and KPI reporting. This role is a pivotal cross-functional leadership position, with the opportunity to build and nurture a world-class facilities team that aligns with our growth and supports our scientific mission. Your Key Contributions Strategic Leadership Develop and implement a comprehensive facilities strategy that aligns with company growth, scientific initiatives, and operational risk management. Recruit, mentor, and lead a high-performing facilities organization, fostering a culture of safety, reliability, and continuous improvement. Team Development Directly manage and mentor facility managers, supervisors, and support staff, promoting a collaborative culture focused on employee engagement and professional development. Encourage cross-functional collaboration with business development, technology, finance, legal, and HR teams to drive informed decisions and improvements. Safety and Compliance Establish and maintain enterprise-wide safety standards and compliance across all facilities; lead audits and implement corrective actions. Direct capital planning, lifecycle management, and end-of-life decisions for critical equipment using ROI-driven analyses. Financial Management Oversee multi-site budgets, long-term capital planning, and KPI performance; optimize total cost of ownership. Manage the vendor lifecycle, including RFPs, contract negotiations, service level agreements, and vendor performance evaluations. Operations Excellence Standardize and enhance maintenance processes utilizing documentation, digital tools, and scalable playbooks; champion improvements focused on employee and occupant satisfaction. Implement governance, risk management, and compliance controls to ensure audit readiness and transparent reporting. Stakeholder Engagement Act as the primary liaison with clients, senior leadership, the Facilities Organization, and key business teams, translating facilities strategy into measurable business value. Collaborate with HR on workforce planning, safety training, and related initiatives.

Your Role at Lila Sciences Lila Sciences stands at the forefront of scientific innovation, operating as the world’s first scientific superintelligence platform and autonomous laboratory dedicated to life sciences, chemistry, and materials science. Our mission is to revolutionize the process of scientific discovery by seamlessly integrating AI into every facet of the scientific method, empowering researchers to address humanity’s most pressing challenges in health, climate change, and sustainability at unprecedented speed and scale. Position Overview As the Director/Senior Director of Applied AI, you will spearhead the establishment of our foundational Applied AI team, responsible for refining and adapting our AI models for practical product deployment. You will ensure their safe integration with diverse customer datasets and oversee the development of high-performance interfaces, including chat experiences and inference endpoints like gRPC, HTTP, and PCP servers. Reporting directly to the CTO, you will manage the complete roadmap from data acquisition to model deployment, collaborating closely with Research, Product, Software, Application, Safety, and Security teams to deliver models that are functional, quantifiable, and dependable. Key Responsibilities Lead and mentor a high-performing Applied AI team to produce exceptional scientific reasoning models for consumer applications. Manage an end-to-end model customization pipeline to generate impactful models from Lila’s base models for high-value applications, including inference, chat, and API integration. Develop a comprehensive evaluation framework to facilitate ongoing model enhancement and performance optimization. Collaborate with cross-functional teams to define project requirements, deliver customer proofs of concept (POCs), and transition successful pilots into scalable products. Establish technical standards, documentation, and incident response protocols for AI systems in production. Recruit, mentor, and foster a diverse and inclusive team environment. Qualifications for Success 8+ years of experience in applied machine learning or ML systems, with a minimum of 3 years in a leadership role; proven track record of deploying large language models (LLMs) into production. Extensive experience in fine-tuning and evaluating large-scale models for customer interactions. Production inference expertise, including familiarity with serving frameworks (Triton, vLLM, TGI, Ray, Kubernetes), GPU orchestration, caching, and observability. Strong understanding of data privacy and security best practices in multi-tenant systems. Preferred Qualifications Experience with instruction fine-tuning and optimization techniques. Proficiency in developing chat user experiences, implementing guardrails, tool/function calling, and managing long-context interactions.

About Flagship Pioneering, Inc. Flagship Pioneering is at the forefront of innovation, dedicated to inventing and nurturing platform companies that have the potential to revolutionize human health, sustainability, and more. Since our inception in 2000, we have successfully launched over 100 companies that tackle some of the world's most pressing challenges, such as vaccinating billions against COVID-19, curing difficult diseases, enhancing human health, preventing illness, and improving agricultural resilience and sustainability. Our commitment to impactful innovation has earned us recognition on FORTUNE's 'Change the World' list, highlighting companies that make a significant social and environmental impact, and we have appeared on Fast Company's annual list of the World’s Most Innovative Companies. Position Summary: We are looking for a passionate and experienced individual to join our Communications and Public Affairs team as the Senior Director of Communications. In this role, you will spearhead the development and implementation of communications and branding strategies for a selection of companies within Flagship Pioneering's diverse portfolio. The ideal candidate will possess a robust background in biotech corporate communications and excel in a fast-paced, startup atmosphere. This is a remarkable opportunity to influence the trajectory of groundbreaking life sciences and technology firms across human health, agriculture, and AI sectors. This full-time role requires in-office presence four days a week in Cambridge, MA. Key Responsibilities: Provide strategic counsel to the founders and leadership of emergent Flagship companies (Flagship NewCos) in developing their brand, voice, foundational messaging, and overall communication strategies. Oversee brand development, visual identity, and website design for NewCos, collaborating with external agencies. Create and implement tailored, integrated communication strategies for company launches, encompassing all written content, media engagement, and social media components. Manage PR agency support as necessary. Develop and execute communication strategies for both NewCos and more established companies (Flagship GrowthCos), including milestone announcements, internal communications, social and digital media strategies, speaking opportunities, and issue management, in close collaboration with company leadership.

Scholar Rock is a pioneering biopharmaceutical entity dedicated to the discovery, development, and delivery of transformative therapies aimed at addressing significant unmet medical needs. As a recognized leader in the biology of the transforming growth factor beta (TGFβ) superfamily, and inspired by the structural resemblance of a scholar rock to protein formations, our clinical-stage company is devoted to advancing groundbreaking treatments that leverage protein growth factors. Over the last decade, we have established a robust pipeline designed to redefine the standard of care for conditions such as neuromuscular diseases, cardiometabolic disorders, and cancer, where growth factor-targeted therapies can make a substantial impact. Scholar Rock stands out as the sole organization demonstrating clinical proof of concept for a muscle-targeted therapy in spinal muscular atrophy (SMA). Our commitment to unlocking innovative therapeutic pathways is underscored by the extensive application of our proprietary platform, which has yielded novel monoclonal antibodies to selectively modulate protein growth factors. By harnessing cutting-edge scientific advancements in traditionally underserved disease areas, we strive each day to create new possibilities for patients. Discover more about our mission at ScholarRock.com and connect with us on @ScholarRock and LinkedIn.Position Overview:As Scholar Rock embarks on a pivotal phase with the impending launch of our inaugural commercial product, we are in search of a strategic and operationally-savvy Senior Director of Global Facilities. This role transcends purely administrative functions; we require a visionary builder who comprehends the intricacies of scaling infrastructure within a rapidly evolving biotech setting while adeptly navigating day-to-day operational challenges.With facilities strategically located worldwide and poised for future growth, you will be responsible for ensuring our environments are safe, compliant, efficient, and conducive to supporting both research and commercial initiatives. If you are a proactive self-starter who thrives in dynamic, transformative organizations and is eager to contribute significantly, this opportunity allows you to apply your expertise, learn extensively, and make a meaningful impact.

The Opportunity: Join Relay Therapeutics as a Senior Medical Director, where you will be pivotal in propelling our clinical pipeline from IND to proof of concept and ultimately to registration. In this role, you will partner with senior medical staff to shape clinical strategies, design clinical trials, and ensure successful execution. Collaborating across various functions including clinical project management, regulatory affairs, clinical operations, biostatistics, data management, and medical writing, you will significantly contribute as Relay Therapeutics continues to advance product candidates into clinical settings. You will provide clinical leadership to R&D teams and closely collaborate with Development leadership. We are open to remote employees

About Fulcrum Therapeutics Fulcrum Therapeutics, Inc. (NASDAQ: FULC) is a clinical-stage biopharmaceutical company based in Cambridge, MA. The team focuses on developing small molecule therapies for genetically defined rare diseases, with an emphasis on areas where patients have limited treatment options. The lead program, Pociredir, aims to increase fetal hemoglobin expression as a novel approach for treating sickle cell disease (SCD). Role Summary: Director of Biostatistics The Director of Biostatistics plays a key role within the Biometrics Department and reports to the VP of Biometrics. This position acts as the statistical subject matter expert for Fulcrum’s clinical development programs and individual studies. The director oversees statistical activities for outsourced clinical trials and ensures all work meets regulatory requirements. Main Responsibilities Serve as the lead statistician for clinical development programs and studies Oversee statistical activities in outsourced clinical trials Ensure compliance with regulatory standards in all statistical work Apply advanced study designs and statistical methods, including estimand strategies, endpoint selection, and approaches for missing data and multiplicity Work closely with teams across biometrics, clinical development, clinical operations, pharmacovigilance, medical writing, and regulatory affairs

Role Overview Lila Sciences is hiring a Director or Senior Director of Talent Acquisition in Cambridge, MA. This leader will guide the full recruitment function, shaping hiring strategy and team structure as the company grows. What You Will Do Lead and mentor the talent acquisition team, setting clear goals and supporting professional development Design and refine recruitment processes to attract and retain skilled professionals in biotechnology Develop strategies to build a diverse and creative workforce Collaborate with leadership to align hiring plans with company objectives About Lila Sciences Lila Sciences advances work in the biotechnology sector from its Cambridge, MA headquarters. The company values innovation, inclusion, and building strong teams to support its mission.