Associate Director, eCOA Technologies
Job Overview
The Associate Director, eCOA Project Management is responsible for leading complex eCOA programs, ensuring successful delivery across scope, timeline, and quality expectations. This role combines hands-on project leadership, people management, and process improvement, with accountability for both project execution and team performance.
You will oversee project managers, support escalations, contribute to account leadership activities, and drive operational excellence across the portfolio. The role is remote within the EU. There may be occasional travel.
Key Responsibilities
- Define and validate project/program scope, timelines, and success metrics for complex eCOA implementations
- Lead end-to-end project delivery, including scope, schedule, cost, and quality management
- Identify risks and develop mitigation strategies; track and report portfolio performance
- Manage and mentor a team of project managers (up to 10 direct reports)
- Conduct regular one-on-ones, manage performance, and support career development of team members
- Act as first point of escalation for project and team-related issues
- Support account leadership and client deliverables as needed
- Partner with stakeholders to ensure alignment on project goals and outcomes
- Lead or contribute to process improvement initiatives and SOP development
- Drive change management, including training coordination and onboarding of new team members
- Deliver presentations and communicate project updates to leadership and cross-functional teams
Qualifications
- Bachelor’s degree in Computer Science, Life Sciences, or a related field (or equivalent experience)
- Approximately 5+ years of direct people management experience preferred
- Strong project management experience in clinical technology or eCOA (preferred but not required if project management expertise is strong)
- Demonstrated experience managing complex programs and cross-functional teams
- Excellent communication and presentation skills (including PowerPoint, Teams, and stakeholder engagement)
- Ability to manage multiple priorities in a fast-paced, evolving environment
Nice to Have
- Familiarity with IRT or eConsent platforms
This role is not eligible for UK visa sponsorship.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Seen 19 days ago.
Original posting on IQVIA's site ↗
Posting text belongs to the employer. Removal requests: contact us.
Nearby
Live postings like this one
Same employer first, then the same role elsewhere.
- 1d ago
- 1d ago
Clinical Research Coordinator -Centro Integrado de Pesquisa _ São José do Rio Preto Full time & Fix Term
São Paulo, Brazil
1d agoMedTech Women's Health Procedural Specialist / Mammographer/Breast Sonographer per diem- Minneapolis/Chicago
Carlsbad CA United States of America
1d ago- 1d ago
Assistente Administrativo de Pesquisa Clínica - Vaga Exclusiva para Pessoas com Deficiência
São Paulo, Brazil
1d ago- 1d ago
- 1d ago
One job at a time
One posting. One CV. $25.
Pick the job you actually want and we write for it.