Associate Director, Study Operations, Rater Services (Spain)

iqvia· IQVIA Information, S.A. (ES51)
Apply Now ↗
📍 Barcelona, SpainFull time
Full timeIQVIA Information, S.A. (ES51)

About this role

Job Overview
Associate Clinical Project Management Directors supervise, manage and provide oversight to assigned Clinical Project Management staff who manage or support studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction. Manage direct reports and teams in accordance with organization's policies and applicable regulations. Ensure direct report employees are fully trained; individual development is aligned; and in place to meet project and organizational needs. Able to attract; develop and retain talent.

Role & Responsibilities

  • Serve as the Principal (or Person) in Charge (PIC) for Cronos projects, providing overall leadership and accountability for project initiation, execution, and closeout.

  • Oversee project governance, ensuring compliance with Cronos and IQVIA policies, SOPs, and regulatory requirements.

  • Lead, mentor, and develop a team of Project Managers and Project Manager Analysts, providing guidance, support, and professional development opportunities.

  • Allocate resources, balance workloads, and ensure optimal team performance across multiple projects.

  • Facilitate project governance reviews, risk assessments, and issue escalation processes.

  • Act as the primary point of contact for senior/executive management regarding project status, risks, and escalations.

  • Ensure accurate and timely completion of project deliverables, including financial reconciliation, documentation, and archiving.

  • Provide operational consultation on all aspects of the Cronos service offering.

  • Drive process improvement initiatives and champion best practices in project management and operational excellence.

  • Represent Cronos Study Operations in cross-functional initiatives and strategic planning.

  • Support business development activities as needed, including proposal development and client presentations.

Required Knowledge, Skills, and Abilities

  • Proven leadership and people management skills, with experience overseeing project teams.

  • Strong knowledge of project governance, risk management, and compliance in a clinical research environment.

  • Excellent problem-solving skills and attention to detail.

  • Strong computer skills, including Microsoft Office applications; experience with project management tools (e.g., Smartsheet, SAP, SharePoint) preferred.

  • Ability to build strong business relationships and influence stakeholders at all levels.

  • Excellent written and oral communication skills.

  • Ability to manage multiple priorities in a fast-paced, dynamic environment.

  • Strong commitment to quality and continuous improvement.

Minimum Required Education and Experience

  • Bachelor’s degree in life sciences, business, or related field (Master’s preferred).

  • 7+ years of experience in clinical research, project management, or study operations, with at least 3 years in a leadership role.

  • Demonstrated experience in project governance, process improvement, and team management.

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.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Frequently Asked Questions

Is the salary disclosed for the Associate Director, Study Operations, Rater Services (Spain) position at iqvia?
The salary for this Associate Director, Study Operations, Rater Services (Spain) role at iqvia is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Associate Director, Study Operations, Rater Services (Spain) position at iqvia located?
This Associate Director, Study Operations, Rater Services (Spain) role at iqvia is based in Barcelona, Spain. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Associate Director, Study Operations, Rater Services (Spain) role at iqvia full-time or part-time?
This is listed as a Full time position. It is posted as a Associate Director, Study Operations, Rater Services (Spain) role in the IQVIA Information, S.A. (ES51) department at iqvia.
Which team or department does the Associate Director, Study Operations, Rater Services (Spain) at iqvia belong to?
This Associate Director, Study Operations, Rater Services (Spain) position is part of the IQVIA Information, S.A. (ES51) department at iqvia. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Associate Director, Study Operations, Rater Services (Spain) position at iqvia?
Click the "Apply Now" button on this page. You will be redirected to iqvia's official application portal hosted on workday where you can submit your application directly.
When was the Associate Director, Study Operations, Rater Services (Spain) job at iqvia posted?
This Associate Director, Study Operations, Rater Services (Spain) position at iqvia was posted on Aug 26, 2026. Apply as soon as possible — early applications are often reviewed first.
Associate Director, Study Operations, Rater Services (Spain)
iqvia
Apply for this role ↗

You'll be redirected to iqvia's official application page on Workday.