Clinical Trials Project Manager

sition Overview:

As a Clinical Trials Project Manager at Datavant, you will be instrumental in the successful implementation of clinical trial tokenization, significantly improving real-world data (RWD) linkage for our Life Science clients. This role offers a unique opportunity to influence the delivery of impactful trial tokenization across the healthcare sector through close collaboration with internal teams and external stakeholders.

Your Responsibilities:

Project & Program Leadership
• Oversee the full implementation of tokenization solutions for clinical trials, ensuring alignment with study goals and regulatory requirements.
• Develop project roadmaps, timelines, and deliverables to achieve timely execution and effective risk management.
• Act as the primary liaison between internal teams (such as product, technical solutions, and engagement management) and external sponsors, CROs, and EDC partners.

Client Engagement
• Work collaboratively with account teams to create and implement training and measurement strategies for trial tokenization solutions.
• Serve as a trusted advisor to sponsors' clinical study teams, providing education on Datavant's tokenization strategies.
• Coordinate with Customer Support for trial setup, configuration, and user management.
• Standardize training programs, content, SOPs, and best practices to ensure smooth adoption of solutions, while iterating based on feedback.
• Manage the portfolio of trial tokenization activities across sites and sponsors.
• Provide transparent communication of progress and outcomes to leaders and stakeholders.

Operational Excellence & Continuous Improvement
• Define and track key performance indicators (KPIs) associated with tokenization adoption.
• Lead improvements in tokenization processes by leveraging emerging technologies and industry insights.
• Collaborate with compliance, legal, and data privacy teams to safeguard patient privacy throughout all processes.
• Support audit readiness and contribute to regulatory submissions and quality assurance efforts.
• Partner with IT and security teams to validate system security and integration with EDC, EHR, and RWD sources.

Qualifications for Success:
• Deep understanding of the Life Sciences industry, especially in clinical development.
• Experience working with clinical operations stakeholders in life sciences organizations or CROs.
• Demonstrable history of leading clinical trial project and engagement management.
• Strong ability to manage scope, timelines, tasks, and project risks effectively.
• Experience collaborating with cross-functional teams and technical experts.
• Flexible in transitioning between leadership and team member roles in dynamic environments.
• A continuous improvement mindset with a commitment to innovation.
• Must be based in EST.

Additional Qualifiers:
• Familiarity with clinical trial sponsors.
• Genuine interest in leveraging data to improve healthcare outcomes.
• Understanding of privacy regulations such as ICH-GCP, GDPR, and HIPAA, among others.
• Knowledge of real-world data or patient tokenization practices.
• Project management certifications like Scrum, PMP, or CCRA are advantageous.
• Preference for candidates in the Greater NYC or Boston area.

At Datavant, we celebrate diversity and are committed to cultivating a high-performance culture where everyone feels valued and empowered. We are proud to be an Equal Employment Opportunity employer.

The estimated total cash compensation for this role is $100,000-$125,000 USD. In our commitment to patient and staff safety, health screenings and vaccinations may be required post-offer.

This position does not offer employment sponsorship.

We are dedicated to a discrimination-free workplace and will consider all qualified applicants based solely on their merit.