Datavant

Trials Delivery Manager, Life Sciences

Datavant$100K — $125K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of experience in life sciences and clinical development
  • Strong background in project and engagement management specific to clinical trials
  • Proven ability to manage complex projects with multiple stakeholders
  • Experience with clinical operations in life sciences organizations or CROs
  • Knowledge of industry regulations such as ICH-GCP, GDPR, and HIPAA
  • Excellent communication and cross-functional collaboration skills
  • Living in the EST zone, preferably Greater NYC or Boston area

Responsibilities

  • Lead the implementation of clinical trial tokenization solutions from start to finish
  • Develop detailed project roadmaps and timelines for execution
  • Act as the main contact for internal teams and external clinical trial partners
  • Build training and measurement plans for trial tokenization solutions
  • Guide clinical study teams on tokenization strategies and process navigation
  • Standardize and improve training programs based on customer feedback
  • Monitor project performance and communicate progress to stakeholders

Benefits

  • Comprehensive rewards strategy that supports high-growth performance
  • Health screenings and vaccination requirements for safety
  • Opportunities for professional growth in a transformative health care environment
  • Engagement with innovative data logistics products and services
  • Potential remote work and flexibility, depending on role
Full Job Description
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 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.

About Datavant

Datavant is a healthcare technology company that specializes in connecting and standardizing healthcare data from various sources. The company's products are used to improve patient care, accelerate drug development, and enhance clinical research. Datavant's platform, called the Datavant Platform, uses artificial intelligence and machine learning to identify and link patient data across different sources while maintaining patient privacy. The company was founded in 2017 by Travis May and is headquartered in San Francisco, California.
Learn more about Datavant
Size
100 employees
Industry
Founded
2017

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