Data Management Quality Associate

The Associate Director of Data Strategy and Governance is responsible for spearheading the University’s data governance initiatives. This role collaborates with senior leaders and data stewards to cultivate a data-driven culture, enhancing best practices in metadata management, data quality, and data security. This position plays a crucial role in elevating Harvard’s overall data maturity.Reporting to the Associate Provost for Institutional Research & Analytics and working closely with the AVP for Administrative Technology Services in HUIT, the Associate Director will coordinate efforts with both OIRA and HUIT to meet the data needs of the entire University.Key Responsibilities:This role is integral in uniting stakeholders across the University to address pressing data-related challenges, while establishing mechanisms to safeguard and strategically utilize our data. As the University’s data maturity progresses, the responsibilities of the Associate Director may adapt accordingly.Organizational Development & Communications:Lead and recruit members for the Executive Data Committee (EDC), University Data Advisory Group (UDAG), and Data Stewardship Council (DSC).Establish effective communication channels regarding data initiatives across various schools and departments and build a thriving community of practice among data stewards.Develop and sustain a curriculum for data governance training for data stewards and other key stakeholders.Enhance executive support for data governance initiatives throughout the University.Deliver strategic updates on data initiatives to various University stakeholders.Engage in thought leadership discussions and forums on data strategy and governance in higher education.Data Strategy Development:Collaborate in creating an enterprise data strategy for the University, taking the lead on project management to track progress toward its goals.Facilitate the identification, development, and promotion of strategic data initiatives.Data Governance Execution:Establish data governance standards, policies, procedures, and best practices, and create a framework to disseminate these practices among stakeholder groups.Improve the University’s management of metadata (e.g., data definitions, data lineage) across diverse data sources.Collaborate with the Information Security and Data Privacy (ISDP) team on data security and privacy efforts, ensuring compliance with regulations.

Your Impact at Lila Sciences Lila Sciences is seeking a highly experienced Director of Federal Strategy and Capture to leverage senior agency relationships and deep knowledge of policy to establish impactful government partnerships and achieve funding successes. As a key member of our Government Partnerships team, you will play a crucial role in shaping the competitive landscape before formal opportunities arise, assessing the trajectory of the federal funding environment, and facilitating connections that require authentic scientific and policy expertise. This position focuses on capture strategy rather than policy development, and requires an individual with extensive federal experience. What You Will Be Building Named Account Ownership - Cultivate, manage, and elevate senior relationships with agencies such as DOE, ARPA-E, NIH, and other relevant U.S. mission agencies, ensuring the health and growth of these connections over time. Opportunity Shaping - Engage with agencies proactively to influence the development of funding opportunities before they are released as RFPs, aligning them with Lila’s strategic goals. Cross-Agency Narrative Development - Collaborate with the Head of Government Partnerships to connect Lila’s initiatives with national science priorities and create a prioritized federal funding pipeline. Institution Building - Assist in establishing Lila’s federal capture function, including tracking relationships, managing the pipeline, and systematically engaging with agencies over time. What You’ll Need to Succeed Extensive U.S. federal experience at the intersection of science, policy, and strategy, including roles within agencies, the National Security Council, interagency, or equivalent backgrounds. Strong scientific understanding in life sciences, biotechnology, or related fields. A proven ability to translate relationships into tangible outcomes, such as funded programs, formal partnerships, or procurement channels. Experience in establishing new government functions, programs, or divisions from the ground up. Ability to thrive in a dynamic, resource-limited environment where you are building processes as you go. Bonus Points For Familiarity with federal funding mechanisms—such as OTAs, cooperative agreements, SBIRs, and BAAs—and adeptness at positioning a company favorably within each. Established relationships within DOE, ARPA-E, DARPA, BARDA, DoD, NSC, or interagency networks in bioeconomy and biosecurity. Experience in startup environments, particularly within government contracting or partnerships. Salary Range: $168,000 - $238,000 annually.

Amylyx Pharmaceuticals is on a bold mission to revolutionize the treatment of diseases that have significant unmet needs. While others may see obstacles, we actively pursue opportunities with urgency, rigorous scientific methods, and a steadfast commitment to the communities we serve. As a clinical-stage company, we are currently targeting conditions such as post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).Our mission is driven by our talented team, united by core values that include being audacious, curious, authentic, engaged, and accountable, fostering a culture of compassion. At Amylyx, we have assembled a highly experienced group dedicated to action, as the communities we serve cannot afford to wait. If you share our passion and are committed to addressing some of the most challenging problems in medicine, we invite you to explore this opportunity and apply.The OpportunityThe Clinical Data Management team at Amylyx Pharmaceuticals is in search of an Associate Director, Clinical Data Programmer. In this role, you will collaborate across functions to deliver hands-on data management support, programming expertise, and technical leadership. You will be responsible for developing, maintaining, and validating clinical databases, as well as executing computer programs to access, visualize, and report clinical trial data, adhering to clinical plans, ICH guidelines, and regulatory standards. As the Associate Director of Clinical Data Programming, proficiency in programming languages is essential for creating both textual and graphical representations that facilitate data cleaning and review.

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.

Join Amylyx Pharmaceuticals as the Senior Director of Market Access Strategy, where you will lead our efforts to enhance market access for our innovative therapies. This position requires a strategic thinker with a proven track record in developing and executing market access strategies in the biotechnology or pharmaceutical sectors. You will collaborate with cross-functional teams to ensure our products reach the patients who need them most.

Join our dynamic team at Integrated Resources, Inc. as an Associate Director of Pharmacovigilance. In this pivotal role, you will oversee the safety and efficacy of pharmaceutical products, ensuring compliance with regulatory standards and advancing our commitment to patient safety.Your expertise in pharmacovigilance will guide our strategic initiatives, collaborating with cross-functional teams to enhance product safety and regulatory submission processes.

Harvard University is hiring an Associate Director of Strategic Sourcing in IT to shape the university’s approach to acquiring technology resources. This position guides procurement strategy, leads sourcing projects, and works with IT teams to secure solutions that fit Harvard’s evolving needs. What you will do Direct strategic sourcing projects for IT products and services Negotiate contracts and oversee supplier partnerships Work with IT departments to understand their requirements and align procurement activities Promote efficiency and support innovation in technology sourcing Role impact This role contributes to Harvard’s mission by ensuring the university has access to dependable and effective technology. Decisions made in this position will influence operational efficiency and help foster ongoing innovation across campus.

Harvard University is seeking an innovative and strategic Associate Director of Research to lead groundbreaking research initiatives. The ideal candidate will possess a deep understanding of research methodologies, strong leadership skills, and a passion for academic excellence. This role involves collaborating with faculty and students to enhance research output and drive impactful scholarship.

AbbVie is seeking a highly skilled Associate Director to lead our Safety Operations Portfolio. This pivotal role involves overseeing safety operations while ensuring compliance with regulatory requirements. The ideal candidate will possess exceptional leadership skills and a strong background in pharmacovigilance.Join our dynamic team and contribute to advancing healthcare solutions that enhance patient safety and improve health outcomes. This is an exciting opportunity for professionals looking to make a meaningful impact in the pharmaceutical industry.

The Opportunity:Relay Therapeutics is in search of an experienced and strategic regulatory leader to join our expanding regulatory team. In this pivotal role, you will define and implement groundbreaking regulatory strategies aimed at accelerating the development and approval of our innovative pipeline. As the global regulatory lead for relevant project teams, you will develop and execute comprehensive strategies for developmental programs. You will also be the primary liaison with the FDA, leading cross-functional teams to ensure successful domestic and international regulatory submissions, including IND, CTA, NDA, and MAA submissions.Your Role:Collaborate closely with regulatory, research, and development teams to design and implement innovative regulatory strategies for our dynamic programs, including both non-clinical and clinical regulatory strategies tailored to specific products.

Company Overview Fulcrum Therapeutics is an innovative clinical-stage biopharmaceutical organization dedicated to enhancing the quality of life for patients suffering from genetically defined rare diseases that exhibit a significant unmet medical need. Our proprietary product engine is adept at identifying drug targets capable of modulating gene expression to address the underlying causes of gene misexpression. We are currently advancing our flagship asset, FTX-6058 (pociredir), a small molecule engineered to elevate fetal hemoglobin expression for the treatment of sickle cell disease and beta thalassemia. Position Summary The Associate Director of Clinical Science will collaborate closely with the Executive Medical Director and VP of Clinical Development to provide critical support across one or more Clinical Project Teams at Fulcrum Therapeutics. This role is pivotal in ensuring the effective design and execution of Clinical Development Plans, focusing on crafting cost-efficient clinical trials that fulfill the needs of both internal and external stakeholders. The successful candidate will assume responsibility for the scientific oversight of clinical studies, working in partnership with study program leadership and cross-functional team members. This includes the interpretation and communication of clinical trial data, which are crucial for high-quality regulatory submissions. Key responsibilities encompass contributing to the design and execution of company-sponsored clinical trials at all developmental phases, analyzing clinical trial data, and facilitating internal and external communications regarding project plans and progress. The Associate Director will also be involved in safety monitoring and mitigation strategies, as well as making significant contributions to regulatory submissions, publications, and communications of clinical data.

We are seeking a dynamic and experienced Associate Director of Real Estate to join our growing team at Turner Townsend. In this pivotal role, you will lead and manage real estate projects, ensuring the delivery of high-quality outcomes while maintaining client satisfaction. You will work closely with clients to understand their needs, develop strategic plans, and oversee the execution of real estate initiatives. Your expertise in project management and real estate development will be crucial in driving project success.

Nuvalent seeks an Associate Director of Clinical Operations to join the team in Cambridge, MA or work remotely. This leadership role guides the execution of clinical trials, ensuring every step aligns with regulatory standards and internal protocols. The position partners with cross-functional teams to develop and deliver on clinical strategies, overseeing studies from planning through closeout. What you will do Direct clinical trial operations for multiple concurrent studies Maintain compliance with all regulatory requirements and company procedures Work closely with colleagues across departments to create and implement clinical strategies Supervise all aspects of study management, from initiation to completion Oversee budgets, timelines, and resource planning for clinical programs Mentor and guide junior staff within clinical operations Requirements Significant experience in clinical operations and project management Background working in pharmaceutical or biotechnology organizations Demonstrated ability to manage budgets and timelines Experience mentoring or managing team members

Your Impact at LilaWe are seeking a dynamic Community & Ecosystem Growth Strategist who embodies a blend of social strategy, influencer engagement, and active community involvement. In this pivotal role, you will be instrumental in expanding high-quality networks of followers for Lila’s executives and scientific leaders by leveraging critical communities within:Academia and researchRelevant industries (materials, energy, chemicals, therapeutics, biotech, aerospace, and defense)Government and public sector science, technology, and innovation ecosystemsYour efforts will ensure our leaders are perceived as credible and consistent in technical discussions, fostering relationships and attracting sustained attention.What You Will Be BuildingExecutive Presence and Follower GrowthDevelop and implement growth strategies for key executives’ social accounts (X, LinkedIn, Substack, and niche community platforms).Expand networks with the right followers: researchers, lab leaders, R&D decision-makers, open-source contributors, and public sector stakeholders.Establish an executive “always-on” engagement strategy: posts, replies, threads, commentary, and light community interaction.Presence in Frontier Technical CommunitiesEngage with online communities discussing AI-accelerated science, robotics, materials science, life sciences, chemistry, frontier technology, generative AI, and agentic science.Integrate Lila into conversations meaningfully and authentically, especially in skeptical or high-signal discussions.Influencer and Community ActivationForge relationships with credible creators and technical influencers across academia, industry, and government-adjacent networks.Coordinate collaborative events: AMAs, roundtables, briefings, interviews, guest threads, and research highlights that elevate Lila leaders.Thought Leadership EnablementGhostwrite or co-author content with executives and technical leaders while maintaining their distinct voice.Coach leaders on effectively engaging in replies and community threads to build trust over hype.Measure and IterateMonitor executive and brand growth using KPIs to refine strategies.

Harvard University is seeking a dynamic and strategic leader for the position of Associate Director of Development Administration. In this pivotal role, you will be responsible for overseeing various administrative functions within the Alumni Relations and Resource Development departments. You will work closely with senior management to implement effective strategies that enhance our fundraising initiatives and strengthen alumni engagement. Your expertise will be crucial in streamlining operations and ensuring that our development efforts are efficient and impactful.

We are seeking a highly skilled Associate Director of Drug Safety and Pharmacovigilance to join our dynamic team at Nuvalent. This pivotal role involves overseeing drug safety operations, ensuring compliance with regulatory requirements, and enhancing the pharmacovigilance strategy. The ideal candidate will possess a deep understanding of drug safety processes and a passion for advancing patient safety in the pharmaceutical industry.

We are seeking an experienced and strategic Associate Director of Supply Chain Management to join our dynamic team at Korrobio. In this pivotal role, you will oversee the development and execution of supply chain strategies that align with our company objectives. You will lead initiatives to optimize processes, enhance efficiency, and drive cost savings across our supply chain operations.Your leadership will be crucial in fostering collaboration with internal teams and external partners to ensure seamless logistics, procurement, and inventory management. You will also play a key role in driving innovation and implementing best practices within the supply chain function.

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 Sobi as the Associate Director of European Supply Chain Management, where you will play a pivotal role in optimizing and managing our supply chain operations across Europe. You will lead a team of professionals, driving efficiency and ensuring that our products reach patients in a timely and effective manner. This is an exciting opportunity to contribute to the healthcare sector and make a meaningful impact.