Associate Director of Clinical Data Management

Join Acadia Pharmaceuticals as the Associate Director of Clinical Data Management, where you will lead and oversee the clinical data management functions critical to our drug development processes. In this pivotal role, you will ensure data integrity, compliance with regulatory standards, and contribute to the generation of high-quality data for our clinical trials.

Role Overview Acadia Pharmaceuticals is hiring an Associate Director of Clinical Operations. This position is based in either Princeton, New Jersey or San Diego, California. The Associate Director will guide key phases of clinical trials, focusing on high-quality execution and adherence to regulatory requirements. What You Will Do Lead and oversee essential stages of clinical trial operations Ensure all activities meet regulatory and company standards Promote effective collaboration across multiple teams Drive project timelines to support company objectives Take a hands-on approach to managing clinical operations

Join Janux Therapeutics as a Senior Manager of Clinical Data Management, where you will oversee the daily operations of our data management activities. In this pivotal role, you will ensure adherence to regulatory standards and industry best practices, enhancing our operational efficiency. You will also collaborate with vendors to support our oncology clinical trials, ensuring the timely delivery of high-quality data management outcomes.We are looking for a proactive and resourceful professional with extensive hands-on experience in data management within oncology indications. Your expertise will be essential in driving our clinical data processes forward.

Fate Therapeutics is seeking a dynamic and experienced Senior Manager or Associate Director of Project Management to become a vital member of our Global Business Operations team. In this pivotal role, you will collaborate closely with the Development and Technical Operations departments to oversee the complete lifecycle of intricate projects. This position acts as a crucial bridge between operational execution, program development strategies, and portfolio direction across our clinical stage programs. This is a full-time, exempt position based at our corporate headquarters in San Diego, CA, reporting directly to the Vice President of Global Operations.

Join our dynamic team at California Creative Solutions Inc. as a Senior Manager of Data Management in the Pharmaceuticals sector. This full-time role is based in beautiful San Diego and is pivotal in ensuring the integrity and quality of clinical data management for our innovative projects.As a Senior Manager, you will lead the Data Management team, overseeing the design, testing, and implementation of clinical data collection studies. Your expertise will be crucial in managing high-quality data deliverables for regulatory submissions, publications, and due diligence activities in collaboration with Contract Research Organizations (CROs).Key Responsibilities:Collaborate in designing and implementing clinical protocols and data collection systems.Develop and uphold data quality plans.Ensure timely execution of data management timelines for assigned projects.Provide strategic input into protocol designs with a focus on data management.Assist Biostatistics in the evaluation of Statistical Analysis Plans.Identify and resolve data discrepancies using standardized validation systems.Oversee the generation of quality data deliverables for regulatory, publication, and due diligence purposes.Participate in reviewing clinical and regulatory documents to maintain data integrity and quality.Manage projects in collaboration with CROs and lead internal project initiatives.Contribute to the development of standards and process documentation, including SOPs and Work Instructions.Support compliance with industry quality standards and guidelines.Assist in selecting, developing, and evaluating personnel to ensure efficient operations.Engage in the corporate and departmental budget processes and management.Facilitate career development for Data Management personnel.Perform additional duties as required.

Oric Pharmaceuticals is seeking a Director of Clinical Quality Assurance to lead our quality assurance efforts. This pivotal role will involve developing and implementing robust quality systems that comply with regulatory standards. As a key player in our clinical operations, you will ensure the integrity of our clinical trials and contribute to the overall success of our drug development programs.

Job OverviewIambic Therapeutics is in search of a Director of Clinical Supply Chain within the CMC division to spearhead the comprehensive clinical supply strategy and its execution for small molecule programs, guiding them from first-in-human trials through various clinical phases. This pivotal role will involve the development and execution of integrated supply plans, overseeing packaging and labeling operations, and managing global distribution to ensure a consistent supply of investigational products to clinical sites while minimizing waste and controlling costs.The ideal candidate will collaborate closely with Clinical Operations, Regulatory Affairs, Quality Assurance, Project Management, and CMC technical teams to ensure alignment on forecasts and manufacturing schedules, manage vendor performance, maintain inspection-ready documentation, and establish effective IRT/RTSM requirements to guarantee reliable and patient-ready clinical supply execution.Preferred location: San Diego, CA

Veracyte, Inc. is seeking a highly skilled and experienced Director of Data Engineering to lead our data initiatives in San Diego. In this pivotal role, you will be responsible for overseeing the development and management of our data engineering strategy, ensuring the integration of high-quality data solutions that empower our teams and drive business outcomes.

Join Iambic Therapeutics as a Senior Clinical Trial Manager in Clinical Operations, where you will take the lead on early-phase oncology studies, overseeing the entire trial process from initiation to completion. You will collaborate closely with teams in Clinical Development, Regulatory Affairs, Biometrics, and external CROs to ensure that trials are executed with the highest quality standards and are ready for inspections in a dynamic biotech environment.In this role, you will be responsible for vendor management, risk assessment, adherence to timelines and budgets, and fostering cross-functional collaboration to guarantee studies meet global regulatory requirements, ICH-GCP standards, and internal SOPs. Reporting directly to the Director of Clinical Operations, this position is based in San Diego, CA.

As a Clinical Trial Manager at Janux Therapeutics, you will be integral to the strategic planning, execution, and management of clinical trials, ensuring the successful progression from study initiation to completion. This role involves overseeing the activities of Contract Research Organizations (CROs), study vendors, and clinical trial sites while collaborating with essential internal stakeholders to guarantee that clinical trial objectives are met on schedule, within budget, and in compliance with regulatory standards, Good Clinical Practice (GCP) guidelines, and internal Standard Operating Procedures (SOPs). Reporting directly to the Director of Clinical Operations, you will be a vital member of the Clinical Operations team, significantly influencing trial strategy and operational excellence in a dynamic, mission-focused biotech environment.

Janux Therapeutics is on the lookout for a dynamic and driven Research Associate or Senior Research Associate to join our Clinical Immunology team in San Diego, CA. This role is perfect for individuals with a solid background in immunology or oncology, preferably within clinical laboratory or CRO environments. You will play a vital role in executing flow-based assays for our innovative TRACTr and TRACIr clinical programs. We are seeking candidates who possess hands-on expertise in flow cytometry, T cell activation, as well as assay development and optimization. This position emphasizes laboratory work and necessitates strong communication and documentation abilities. A collaborative spirit, self-motivation, and a commitment to achieving excellence are key traits we value in our ideal candidate.

Unlock Your Potential with Access.Join our dynamic team to create and deliver inspiring experiences that connect people and ignite their imagination while enjoying the journey.We are seeking an Associate Managing Director to spearhead growth in our West territory, collaborating closely with executive leadership to enhance performance, cultivate a strong culture, and achieve operational excellence.In this pivotal role, you will co-manage a multi-million-dollar territory and work alongside leaders from Sales, Creative, Events, and Home Office teams to implement the territory’s annual business plan. This strategic leadership position emphasizes business expansion, team development, and operational efficiency.The Associate Managing Director is vital in enhancing territory leadership while developing the financial, strategic, and people leadership skills necessary for advancement to a future Managing Director role.About the RoleAs the Associate Managing Director, you will guide the strategic direction and performance of the territory, oversee P&L management, drive key performance metrics, and build high-performing teams.You will partner with Executive Leadership, Corporate Finance, Talent Operations, and your Managing Director mentor to formulate and execute the territory’s annual business plan while adhering to company guidelines. This role demands robust cross-functional collaboration, operational insight, and strong leadership presence across Sales, Creative, and Events teams.Additionally, the Associate Managing Director serves as a key representative of Access in the local market, fostering relationships with clients, hotels, and strategic partners while contributing to the territory's long-term growth.Key ResponsibilitiesTeam Leadership & Culture DevelopmentLead and guide a talented team of Directors, Associate Directors, and Managers across Sales, Events, and Creative domains, enhancing leadership capacity as the territory expands.Conduct regular one-on-one meetings, monthly reviews, and development plans to ensure leaders receive ongoing coaching, performance feedback, and career advancement support.Cultivate a high-engagement culture that embodies Access values by recognizing outstanding performers, mentoring high-potential team members, and addressing performance issues effectively.

Join HeartFlow, Inc. as a Clinical Trial Manager dedicated to advancing healthcare innovation along the West Coast. In this pivotal role, you will oversee and manage clinical research projects, ensuring compliance with regulatory standards and protocols while collaborating with multidisciplinary teams. You will drive the planning, execution, and management of clinical trials, ensuring the highest quality of data collection, analysis, and reporting.

Why Choose PlayStation?At PlayStation, we pride ourselves on being not just the best place to play, but also the best place to work. As a globally recognized leader in entertainment, we develop the PlayStation family of products and services, including PlayStation®5, PlayStation®4, PlayStation®VR, PlayStation®Plus, and critically acclaimed titles from PlayStation Studios.We are committed to fostering an inclusive environment that empowers our employees and celebrates diversity. We invite passionate and innovative individuals who share our love for technology and gaming to explore our career opportunities and join our expanding global team.The PlayStation brand is part of Sony Interactive Entertainment, a wholly-owned subsidiary of Sony Group Corporation.Position: Senior Director of Data Platform Engineering & OperationsLocation: San Diego, CAAs the Senior Director of Data Platform Engineering & Operations, you will play a pivotal leadership role at Sony Interactive Entertainment (SIE). You will be responsible for spearheading innovation and scalability across our comprehensive data and AI platform ecosystem. This encompasses overseeing our Data Infrastructure (including Streaming, Ingestion, Warehouse, and Data Ocean), Experimentation and Audience Platforms, and Governance & Data Observability tools.In this influential role, you will ensure that SIE's platforms are capable of processing immense data volumes, delivering insights that enhance the experiences of Players, Creators, Publishers, and Enterprises. By enabling data-driven decision-making at scale, you will shape the future of personalized gaming, streamline operations, and boost enterprise productivity through cutting-edge AI and machine learning technologies.As a strategic leader, you will define and implement the vision for SIE's data and AI platform ecosystem, ensuring that our solutions are scalable and align with key business objectives across gaming, content creation, and corporate operations. Reporting directly to the VP of Data & AI, you will lead global teams of engineers and specialists in building platforms that democratize data usage and transform decision-making processes throughout the organization. Candidates with substantial experience in senior leadership roles will be given priority consideration.

Join Amgen as a Clinical Risk Management Manager in San Diego, where you will play a pivotal role in enhancing patient safety and minimizing clinical risks. You will lead initiatives that ensure compliance with regulatory standards while fostering a culture of continuous improvement.

Associate Director of Practice Area - Life Sciences Join Syska Hennessy Group, a global leader in consulting, engineering, and commissioning services, specializing in advanced technical buildings and their essential systems. We are in search of a dynamic, performance-oriented leader to collaborate with our national life sciences and healthcare teams. This role offers the opportunity to oversee and develop our practice area in the Northeast or West region, capitalizing on our established legacy and strong client relationships. In this pivotal position, you will spearhead initiatives to secure and manage pharmaceutical manufacturing, laboratory, and medical device projects. You will oversee the regional life sciences team, guiding the development of strategic business plans and executing a diverse range of projects. This role reports directly to the regional leader of the firm. Our vibrant work environment promotes professional growth, combining a supportive culture, a diverse workforce, competitive compensation, and a flexible work schedule (Monday to Thursday in-office for 9 hours and Friday 4 hours remotely). We also host engaging social events, making it an ideal setting for a fulfilling and challenging career. As a management-owned entity, we are committed to rewarding our key leaders with opportunities for ownership, promoting overall performance and recognition.

Join Iambic Therapeutics as the Associate Director of Drug Metabolism and Pharmacokinetics (DMPK), where you will drive innovative DMPK strategies throughout our discovery and preclinical development programs. Your expertise will be pivotal in designing and implementing integrated ADME/PK strategies that facilitate program advancement and inform critical decision-making for IND submissions.In this role, you will represent DMPK on cross-functional teams, collaborating closely with our internal scientists and external CRO partners to plan, execute, and interpret studies. This position is based at our San Diego Headquarters, where you will be at the forefront of advancing therapeutic candidates. KEY RESPONSIBILITIESDesign and implement DMPK strategies to propel discovery and development initiatives.Plan, execute, and interpret DMPK studies to support the progression of therapeutic candidates during discovery and early development stages.Collaborate with diverse teams including medicinal chemistry, biology, CMC, and clinical to provide DMPK insights that inform project decisions.Utilize AI-driven tools and computational methods to enhance DMPK strategy, facilitate predictive ADME/PK assessments, and expedite data-driven decision-making.Address ADME/PK-related challenges during lead optimization.Oversee external ADME/PK and PK/PD studies, coordinating with CROs and reviewing data.Prepare DMPK summaries and regulatory submission documentation (e.g., IND, IB).Interpret ADME/PK data, communicating findings and recommendations effectively to project teams.Stay abreast of advancements in DMPK, PBPK, PK/PD, and regulatory guidelines.Ensure that all studies comply with relevant regulatory and quality standards.

As the Director of Global Regulatory Affairs at Janux Therapeutics, you will take on a pivotal role in shaping and executing regulatory strategies that facilitate the global development and expansion of our innovative clinical pipeline. This position requires a dynamic leader who can effectively manage teams while collaborating closely with cross-functional departments to ensure adherence to regulatory standards and achieve successful approval outcomes.

Join Janux Therapeutics as the Senior Executive Director of Clinical Pharmacology, where you will play a pivotal role in shaping our clinical development programs. We are looking for a proactive, data-driven leader who excels in the design, analysis, and interpretation of clinical pharmacology strategies. This position is perfect for a scientific innovator who enjoys working closely with data to ensure exemplary pharmacokinetic (PK) analyses and facilitates informed decision-making regarding dosage selection and regulatory submissions.In this role, you will prioritize executional excellence and strategic alignment within the team, ensuring that all deliverables meet the highest standards of scientific rigor.

About Acadia Pharmaceuticals Acadia Pharmaceuticals is dedicated to transforming scientific potential into impactful innovations that greatly benefit underserved communities affected by neurological and rare diseases globally. Our diverse commercial portfolio proudly includes the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are committed to pioneering the next generation of therapeutic advancements, supported by a robust pipeline featuring mid- to late-stage programs targeting Alzheimer’s disease psychosis and Lewy body dementia psychosis, alongside early-stage initiatives addressing additional unmet patient needs. At Acadia, we strive to be the catalyst for change in these communities.This position can be based in Princeton, NJ, or San Diego, CA, with our hybrid work model requiring an average of three days per week in the office.Position SummaryThe Senior Director of Commercial Advanced Analytics & Data Strategy holds a pivotal leadership role tasked with defining, developing, and expanding the analytics capabilities, data strategy, and governance frameworks that empower commercial decision-making throughout the organization. This role ensures the seamless integration of high-quality data, advanced analytics, and AI-driven insights into commercial strategy, planning, execution, and market optimization. The Senior Director acts as a strategic collaborator across functions, translating business priorities into scalable analytics products and platforms while ensuring governance, compliance, and measurable business outcomes.Over time, this position will cultivate and enhance our commercial advanced analytics and data capabilities, establish effective operating models, and outline future talent and capability demands to support our evolving business landscape. The role will closely collaborate with Acadia’s AI team, which provides shared AI expertise across Commercial and R&D, as well as IT teams responsible for enterprise data, infrastructure, and platform enablement.Primary ResponsibilitiesCommercial Analytics Strategy & LeadershipPartner with Commercial leadership to define the advanced analytics vision, strategy, and initiatives that enable decision-making and performance optimization.