Clinical Trial Manager

Datavant is the data collaboration platform trusted for healthcare. Guided by our mission to make the world’s health data secure, accessible and actionable, we provide critical data solutions for organizations across the healthcare ecosystem - including providers, health plans, researchers, and life sciences companies. From fulfilling a single patient’s request for their medical records to powering the AI revolution in healthcare, Datavanters are building the future of how data is connected and used to improve health. By joining Datavant today, you’re stepping onto a driven and highly collaborative team that is passionate about creating transformative change in healthcare. What We’re Looking For: As a Datavant Trials Delivery Manager, you will play a critical role in driving the successful implementation of clinical trial tokenization to enable RWD linkage for Datavant’s Life Science customers. You will partner with internal and external stakeholders across engagement management, product, technical solutions, and sales, to ensure that our clinical trial solutions drive real, measurable impact for customers. This is not just a project management role - it’s an opportunity to shape how trial tokenization is delivered at scale across the healthcare industry. What You Will Do and Own: Project & Program Leadership Lead the end-to-end implementation of tokenization solutions for Datavant-contracted clinical trials, ensuring alignment with study objectives and regulatory / compliance requirements. Develop project roadmaps, timelines, and key deliverables, ensuring on-time execution and risk mitigation. Serve as the primary liaison between internal teams (e.g., product, technical solutions, engagement management, and sales) and external life sciences sponsors, contract research organizations (CROs), and eClinical / EDC partners Client Engagement Work with Datavant account teams to build and implement robust training and measurement plans for our trial tokenization solutions for each Sponsor Work with sponsor’s clinical study teams to be their trusted advisor, to educate and guide them on Datavant tokenization strategies and tactics - support and navigate ongoing questions to provide timely and quality resolution to customer needs Coordinate with Customer Support on all trial setup, configuration, and user access mgmt Standardize trial tokenization training programs, content, SOPs, and best practices to ensure smooth adoption across clinical teams - improve and iterate based on customer feedback and market learnings Program manage portfolio of trial tokenization activities by site and sponsor Track and communicate progress and outcomes to leadership, sponsors, and external stakeholders. Operational Excellence & Continuous Improvement Define key performance indicators (KPIs) and monitor tokenization adoption across research sites Develop, implement, and drive continuous improvement in enterprise level approaches to tokenization, leveraging emerging technologies and industry trends. Collaborate with engagement management, compliance, legal, and data privacy teams to support processes that safeguard patient privacy, instilling confidence in customers and study teams Support audit readiness and contribute to regulatory submissions, inspections, and internal quality assurance processes. Work with IT and security teams to validate system security, interoperability, and integration with electronic data capture (EDC), electronic health records (EHR), and real-world data (RWD) sources What You Need to Succeed: Understanding of the Life Sciences industry, with a focus on clinical development Prior experience working with clinical operations stakeholders at life sciences organizations, contract research organizations, and/or eClinical partners Prior experience leading the scoping and delivery of clinical trial engagements including comprehensive project and engagement management related to clinical data management or healthcare technology implementation Demonstrated competence in scope and expectation management Proven ability to drive project-based work, managing tasks, schedules deliverables, budgets, and project risks, in an agile and fast-paced environment Experience collaborating with cross-functional teams and technical subject matter experts in a manner that fosters a productive environment for the project team Demonstrated flexibility and effectiveness in both leadership and team member roles in dynamic environments Continuous improvement mindset and ability to build, define, and iterate Must live in EST What Helps You Stand Out: Direct experience working at a Clinical trial sponsor A passion for leveraging data to drive better healthcare outcomes Familiarity with ICH-GCP, GDPR, HIPAA, 21 CFR Part 11, or other privacy regulations Familiarity with real-world data and / or patient tokenization Project management certification eg. Scrum, PMP, CCRA Preference given for candidates located on the East Coast and in the Greater NYC or Boston area #LI-BC1 We are committed to building a diverse team of Datavanters who are all responsible for stewarding a high-performance culture in which all Datavanters belong and thrive. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. At Datavant our total rewards strategy powers a high-growth, high-performance, health technology company that rewards our employees for transforming health care through creating industry-defining data logistics products and services. The range posted is for a given job title, which can include multiple levels. Individual rates for the same job title may differ based on their level, responsibilities, skills, and experience for a specific job. The estimated total cash compensation range for this role is: $100,000—$125,000 USD To ensure the safety of patients and staff, many of our clients require post-offer health screenings and proof and/or completion of various vaccinations such as the flu shot, Tdap, COVID-19, etc. Any requests to be exempted from these requirements will be reviewed by Datavant Human Resources and determined on a case-by-case basis. Depending on the state in which you will be working, exemptions may be available on the basis of disability, medical contraindications to the vaccine or any of its components, pregnancy or pregnancy-related medical conditions, and/or religion. This job is not eligible for employment sponsorship. Datavant is committed to a work environment free from job discrimination. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. To learn more about our commitment, please review our EEO Commitment Statement here ( . Know Your Rights ( , explore the resources available through the EEOC for more information regarding your legal rights and protections. In addition, Datavant does not and will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay. At the end of this application, you will find a set of voluntary demographic questions. If you choose to respond, your answers will be anonymous and will help us identify areas for improvement in our recruitment process. (We can only see aggregate responses, not individual ones. In fact, we aren’t even able to see whether you’ve responded.) Responding is entirely optional and will not affect your application or hiring process in any way. Datavant is committed to working with and providing reasonable accommodations to individuals with physical and mental disabilities. If you need an accommodation while seeking employment, please request it here, ( by selecting the ‘Interview Accommodation Request’ category. You will need your requisition ID when submitting your request, you can find instructions for locating it here ( . Requests for reasonable accommodations will be reviewed on a case-by-case basis. For more information about how we collect and use your data, please review our Privacy Policy ( . #J-18808-Ljbffr