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Associate Director Validation Jobs in Roxboro, NC

... Validation. The Associate Director, Engineering is responsible for the maintenance and reliability of both utilities and process equipment. The scope of responsibilities includes maintenance and ...

Quality Control Analyst II

Durham, NC

$23.25 - $31.25/hr

This position is based on site in Durham, NC and reports to the Associate Director, Quality Control ... All employment decisions are based on valid jobrelated requirements. If you are a qualified ...

Quality Control Analyst

Durham, NC · On-site

$23.25 - $31.25/hr

This position is based on site in Durham, NC and reports to the Associate Director, Quality Control ... All employment decisions are based on valid job-related requirements. If you are a qualified ...

Quality Control Analyst II

Durham, NC · On-site

$23.25 - $31.25/hr

This position is based on site in Durham, NC and reports to the Associate Director, Quality Control ... All employment decisions are based on valid job-related requirements. If you are a qualified ...

Quality Control Analyst

Durham, NC

$23.25 - $31.25/hr

This position is based on site in Durham, NC and reports to the Associate Director, Quality Control ... All employment decisions are based on valid jobrelated requirements. If you are a qualified ...

This position is office-based in RTP, NC and will report to Associate Director, Facilities ... All employment decisions are based on valid job-related requirements. If you are a qualified ...

This position is office-based in RTP, NC and will report to Associate Director, Facilities ... All employment decisions are based on valid jobrelated requirements. If you are a qualified ...

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Associate Director Validation information

See Roxboro, NC salary details

$26.8K

$90.4K

$152.2K

How much do associate director validation jobs pay per year?

As of Jul 8, 2026, the average yearly pay for associate director validation in Roxboro, NC is $90,370.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,600.00 and $124,000.00 per year, depending on experience, location, and employer.

How does an Associate Director of Validation typically collaborate with cross-functional teams during major projects?

An Associate Director of Validation works closely with departments such as Quality Assurance, Manufacturing, Engineering, and Regulatory Affairs to ensure that validation activities meet both internal standards and regulatory requirements. This often involves leading multi-disciplinary project teams, facilitating communication, and resolving challenges related to process or equipment validation. Regular meetings, joint risk assessments, and coordinated documentation are common, which helps streamline project timelines and maintain compliance. Effective collaboration is essential for successful product launches and ongoing process improvements.

What is the difference between Associate Director Validation vs Validation Manager?

AspectAssociate Director ValidationValidation Manager
CredentialsBachelor's or Master's in Life Sciences, Engineering, or related fields; often requires industry certificationsBachelor's or Master's in similar fields; certifications like ASQ or ISPE are common
Work EnvironmentLeads validation teams, oversees validation strategies, and collaborates with cross-functional departmentsManages validation projects, ensures compliance, and reports to senior management
Employer & Industry UsagePharmaceutical, biotech, and medical device industries; used in large organizationsSimilar industries; common in mid to large-sized companies for validation oversight

The Associate Director Validation typically holds a higher strategic role, overseeing validation teams and strategies, while the Validation Manager focuses on managing validation projects and ensuring compliance. Both roles require similar credentials and are vital in regulated industries, but the Associate Director has broader leadership responsibilities.

What are the key skills and qualifications needed to thrive as an Associate Director Validation, and why are they important?

To excel as an Associate Director Validation, you need in-depth knowledge of validation principles, regulatory guidelines (such as FDA, EMA), and a background in life sciences or engineering, often supported by advanced degrees. Familiarity with validation software, quality management systems (QMS), and industry-standard protocols like GAMP or ASTM E2500 is crucial. Strong leadership, project management, and cross-functional communication skills help drive teams and ensure compliance. These competencies are essential to maintain product quality, regulatory adherence, and efficient validation processes in a highly regulated environment.

What is an Associate Director of Validation?

An Associate Director of Validation is a leadership role in the pharmaceutical, biotechnology, or medical device industries responsible for overseeing validation activities. This includes ensuring that equipment, processes, and systems meet regulatory standards and function as intended. The Associate Director manages validation teams, develops validation strategies, and ensures compliance with industry regulations such as FDA and GMP. They play a key role in quality assurance and help maintain the integrity of products and processes.
What cities near Roxboro, NC are hiring for Associate Director Validation jobs? Cities near Roxboro, NC with the most Associate Director Validation job openings:
Infographic showing various Associate Director Validation job openings in Roxboro, NC as of July 2026, with employment types broken down into 1% As Needed, 66% Full Time, 30% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $90,370 per year, or $43.4 per hour.
Associate Director, eCOA Project Management

Associate Director, eCOA Project Management

IQVIA

Durham, NC • Remote

$100K - $278K/yr

Full-time

Posted 20 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

53rd of 207 rated it services


Job description

Join a high-growth team at the forefront of eCOA delivery, where you'll lead complex, global clinical programs that directly impact patient-centric research. As an Associate Director, you'll take on a highly visible leadership role-driving project excellence, mentoring teams, and shaping operational strategy in a dynamic and evolving environment.

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 with occasional travel and a preference for Eastern Time Zone alignment.

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 (approximately 7-8 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

  • eCOA systems experience
  • Familiarity with IRT or eConsent platforms

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 athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

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.

The potential base pay range for this role, when annualized, is $100,200.00 - $278,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US