Executive Director, Data & Technology Site & Study Start Up
Parexel International, Little Rock, Arkansas, United States, 72208
Overview
Parexel is looking for changemakers who are driven by curiosity, passion, and optimism. Come join us in keeping the Patient at the Heart of Everything We do.
Job Title : Executive Director, Data & Technology Site & Study Startup Support
Job Purpose:
The
Executive Director, D&T Site & Study Startup Support
serves as the senior technology and data leader partnering with Parexel’s global
Site & Study Startup
organization. This role ensures that business teams are fully enabled with efficient, reliable, and compliant technology, data, systems, and process capabilities. This leader ensures optimized delivery of startup activities, higher predictability of activation timelines, improved data quality, and robust operational systems across feasibility, regulatory submissions, site activation, and early‑study operational readiness.
Why we are looking for you We’re looking for a dynamic, forward‑thinking innovator with hands‑on experience in clinical operations technology who’s ready to elevate how studies get started and executed. You thrive at the intersection of feasibility, regulatory workflows, submissions, and site activation and you know these processes inside and out. You’ve led the charge on implementing enterprise clinical systems, driving seamless cross‑functional integrations, and ensuring data flows effortlessly across the clinical ecosystem.
Responsibilities
Technology & Process Leadership
Serve as the primary D&T executive partner for the global Site & Study Startup function, ensuring alignment to operational processes and startup lifecycle needs.
Drive system enhancements that improve startup predictability, data capture, cycle times, and risk identification.
Use innovative technology to improve effectiveness and efficiency of the business.
Partner with business leaders to ensure systems availability and support:
Feasibility modeling
Country and site selection
Document collection and workflows
ICF customization
EC/RA/MoH submissions
SIV scheduling and activation readiness
Enablement of Feasibility, Site Identification & Country Strategy
Provide technology, analytical models, and data tools for feasibility assessments, including site intelligence, enrollment scenario modeling, and country strategy inputs
Ensure real‑time access to feasibility insights, performance history, and site data across data platforms.
Integration of Workflows with Operational, Regulatory & Clinical Systems
Oversee integrations between Site & Study Startup systems and broader D&T ecosystem systems
Coordinate with regulatory and compliance technology partners to ensure consistent data flows into the broader D&T architecture.
Ensure end‑to‑end system readiness and integration for:
Regulatory document management
Site regulatory package preparation
Greenlight/activation processes
System setup and training workflows
Operational Reporting, Data Quality & Predictive Insights
Build and scale reporting capabilities that measure startup progress, activation risks, feasibility metrics, and regulatory timelines.
Partner with Data Aggregation & Reporting and Data Governance teams to ensure consistent definitions and quality of
clinical operational data
Introduce predictive analytics to identify bottlenecks and propose mitigation before they impact activation.
System Lifecycle Ownership for SSU Platforms
Govern upgrades, enhancements, compliance validation, testing, and UAT for systems such as feasibility tools, regulatory workflow systems, site activation trackers, and training/access workflows.
Ensure systems meet GxP relevance expectations when applicable, using validation frameworks from the broader D&T quality ecosystem.
Leadership, Strategy & Organizational Enablement
Lead a global team of product owners, business analysts, solution architects, and technologists supporting Site & Study Startup systems and processes.
Collaborate with D&T and business leaders to strengthen business automation and capabilities
Drive operational excellence, customer focus, and continuous improvement across the organization.
Skills
Deep knowledge of site and study startup processes (feasibility, submissions, activation, regulatory workflows).
Strong understanding of clinical operational systems and data flows.
Expertise delivering technology solutions in regulated clinical research environments.
Executive‑level communication, influence, and cross‑functional leadership.
Ability to translate operational challenges into system and data improvements.
Knowledge and Experience
15+ years of experience in clinical operations technology, Site & Study Startup processes, feasibility, regulatory workflows, or related domains.
Experience implementing enterprise clinical systems and managing cross‑functional integrations.
Proven ability leading global, matrixed technology or operational teams.
Education
Bachelor’s degree in Life Sciences, Engineering, Business, or related discipline required.
Master’s degree or equivalent experience preferred.
Why join us
Opportunity to work on innovative projects at the forefront of the industry.
Collaborative and inclusive work environment that values your expertise.
Professional advancement and development opportunities.
Work life balance and flexible working hours.
Parexel Benefits
Health, Vision & Dental Insurance
Tuition Reimbursement
Vacation/Holiday/Sick Time
Flexible Spending & Health Savings Accounts
Work/Life Balance
401(k) with Company match
Pet Insurance
Full list of benefits available here: https://www.parexel.com/us-benefits
About Parexel International At Parexel we embrace flexibility and understand that in today’s fast-paced world, employees need to balance their careers with their personal lives. Come join us where learning is constant, you are exposed to a world of experiences and open doors. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy, and we are committed to making a difference.
If this job does not sound like the next step in your career, but perhaps you know of someone who’d be a perfect fit, please share the job posting link to apply!
#LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
#J-18808-Ljbffr
Job Title : Executive Director, Data & Technology Site & Study Startup Support
Job Purpose:
The
Executive Director, D&T Site & Study Startup Support
serves as the senior technology and data leader partnering with Parexel’s global
Site & Study Startup
organization. This role ensures that business teams are fully enabled with efficient, reliable, and compliant technology, data, systems, and process capabilities. This leader ensures optimized delivery of startup activities, higher predictability of activation timelines, improved data quality, and robust operational systems across feasibility, regulatory submissions, site activation, and early‑study operational readiness.
Why we are looking for you We’re looking for a dynamic, forward‑thinking innovator with hands‑on experience in clinical operations technology who’s ready to elevate how studies get started and executed. You thrive at the intersection of feasibility, regulatory workflows, submissions, and site activation and you know these processes inside and out. You’ve led the charge on implementing enterprise clinical systems, driving seamless cross‑functional integrations, and ensuring data flows effortlessly across the clinical ecosystem.
Responsibilities
Technology & Process Leadership
Serve as the primary D&T executive partner for the global Site & Study Startup function, ensuring alignment to operational processes and startup lifecycle needs.
Drive system enhancements that improve startup predictability, data capture, cycle times, and risk identification.
Use innovative technology to improve effectiveness and efficiency of the business.
Partner with business leaders to ensure systems availability and support:
Feasibility modeling
Country and site selection
Document collection and workflows
ICF customization
EC/RA/MoH submissions
SIV scheduling and activation readiness
Enablement of Feasibility, Site Identification & Country Strategy
Provide technology, analytical models, and data tools for feasibility assessments, including site intelligence, enrollment scenario modeling, and country strategy inputs
Ensure real‑time access to feasibility insights, performance history, and site data across data platforms.
Integration of Workflows with Operational, Regulatory & Clinical Systems
Oversee integrations between Site & Study Startup systems and broader D&T ecosystem systems
Coordinate with regulatory and compliance technology partners to ensure consistent data flows into the broader D&T architecture.
Ensure end‑to‑end system readiness and integration for:
Regulatory document management
Site regulatory package preparation
Greenlight/activation processes
System setup and training workflows
Operational Reporting, Data Quality & Predictive Insights
Build and scale reporting capabilities that measure startup progress, activation risks, feasibility metrics, and regulatory timelines.
Partner with Data Aggregation & Reporting and Data Governance teams to ensure consistent definitions and quality of
clinical operational data
Introduce predictive analytics to identify bottlenecks and propose mitigation before they impact activation.
System Lifecycle Ownership for SSU Platforms
Govern upgrades, enhancements, compliance validation, testing, and UAT for systems such as feasibility tools, regulatory workflow systems, site activation trackers, and training/access workflows.
Ensure systems meet GxP relevance expectations when applicable, using validation frameworks from the broader D&T quality ecosystem.
Leadership, Strategy & Organizational Enablement
Lead a global team of product owners, business analysts, solution architects, and technologists supporting Site & Study Startup systems and processes.
Collaborate with D&T and business leaders to strengthen business automation and capabilities
Drive operational excellence, customer focus, and continuous improvement across the organization.
Skills
Deep knowledge of site and study startup processes (feasibility, submissions, activation, regulatory workflows).
Strong understanding of clinical operational systems and data flows.
Expertise delivering technology solutions in regulated clinical research environments.
Executive‑level communication, influence, and cross‑functional leadership.
Ability to translate operational challenges into system and data improvements.
Knowledge and Experience
15+ years of experience in clinical operations technology, Site & Study Startup processes, feasibility, regulatory workflows, or related domains.
Experience implementing enterprise clinical systems and managing cross‑functional integrations.
Proven ability leading global, matrixed technology or operational teams.
Education
Bachelor’s degree in Life Sciences, Engineering, Business, or related discipline required.
Master’s degree or equivalent experience preferred.
Why join us
Opportunity to work on innovative projects at the forefront of the industry.
Collaborative and inclusive work environment that values your expertise.
Professional advancement and development opportunities.
Work life balance and flexible working hours.
Parexel Benefits
Health, Vision & Dental Insurance
Tuition Reimbursement
Vacation/Holiday/Sick Time
Flexible Spending & Health Savings Accounts
Work/Life Balance
401(k) with Company match
Pet Insurance
Full list of benefits available here: https://www.parexel.com/us-benefits
About Parexel International At Parexel we embrace flexibility and understand that in today’s fast-paced world, employees need to balance their careers with their personal lives. Come join us where learning is constant, you are exposed to a world of experiences and open doors. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy, and we are committed to making a difference.
If this job does not sound like the next step in your career, but perhaps you know of someone who’d be a perfect fit, please share the job posting link to apply!
#LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
#J-18808-Ljbffr