Trials Delivery Manager, Life Sciences
About the role
As a Datavant Trials Delivery Manager, you will play a critical role in driving the successful implementation of clinical trial tokenization to enable real-world data (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 an opportunity to shape how trial tokenization is delivered at scale across the healthcare industry.
Responsibilities
- 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.
- Work with Datavant account teams to build and implement robust training and measurement plans for trial tokenization solutions for each sponsor.
- Act as a trusted advisor to sponsors’ clinical study teams, educating and guiding them on Datavant tokenization strategies and tactics, and resolving ongoing questions.
- Coordinate with Customer Support on trial setup, configuration, and user access management.
- Standardize trial tokenization training programs, content, SOPs, and best practices to ensure smooth adoption across clinical teams, iterating based on customer feedback and market learnings.
- Program manage a portfolio of trial tokenization activities by site and sponsor.
- Track and communicate progress and outcomes to leadership, sponsors, and external stakeholders.
- 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.
- 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.
Requirements
- 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 productive environment.
- 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 the EST time zone.
Qualifications
- Direct experience working at a clinical trial sponsor (preferred).
- 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 (e.g., Scrum, PMP, CCRP).
- Preference given for candidates located on the East Coast and in the Greater NYC or Boston area.
Pay
The estimated total cash compensation range for this role is $100,000—$125,000 USD.
Schedule
This role requires post-offer health screenings and proof/completion of vaccinations such as the flu shot, Tdap, COVID-19, etc. Exemptions may be available on a case-by-case basis for disability, medical contraindications, pregnancy, or religious reasons, depending on state laws.