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IQVIA · Lisbon, Portugal

# Site Activation Specialist-Portugal

Lisbon, Portugal Full-time 

Listed on IQVIA’s official careers site. Posted October 30, 2026. Check that it is still open and apply there.
[Apply on IQVIA’s careers site →](https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Lisbon-Portugal/Site-Activation-Specialist-Portugal_R1567677)

[OpenNash Jobs](https://jobs.opennash.com/) / [IQVIA](https://jobs.opennash.com/companies/iqvia/) / Site Activation Specialist-Portugal

## Job description

### Site Activation Specialist Global Site Activation Location

Portugal Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers. IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication.

We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available.

### Job Overview

As a Site Activation Specialist, you will serve as a Single Point of Contact to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager, Project Management team, and other departments as necessary. You will review documents for completeness, consistency, and accuracy, under guidance of senior staff and prepare site documents, inform team members of completion of regulatory contractual.

Along with distributing completed documents to sites and internal project team member and updating and maintaining internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information. You will also review, track, and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents.

### Requirements and Skills
- Bachelor’s Degree in Life Science or related field
- Minimum of 3 years’ prior experience in Clinical Research Experience with activities such as submissions to Ethics Committees and Regulatory Authorities, contract and budget negotiations, study start-up activities, and overall site activation processes
- Familiarity with the day-to-day responsibilities within Global Site Activation essential
- Ability to work independently but also collaborate with others Good interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsors
- Ability to work on multiple projects
- Knowledge of applicable functional/regulatory requirements, including local regulations, SOPs and ICH/ GCP Join IQVIA and let’s create a healthier world together: Exposure across 21 Therapeutic Areas Be part of a global team who operate across 141 locations Exposure across a variety of studies and projects Access to new, innovative technologies
- Work within a collaborative and vibrant environment
- Own your career!

Unleash your potential! It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world. When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.

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](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.

## At a glance
- Posted by the employer: Oct 30, 2026
- First seen by OpenNash: Oct 31, 2026
- Last checked: Oct 31, 2026
- Listed for: 1 day
- Location: Lisbon, Portugal
- Employment type: Full-time[Apply on IQVIA’s careers site →](https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Lisbon-Portugal/Site-Activation-Specialist-Portugal_R1567677)

## Hiring at IQVIA
- Open jobs: 1,903
- New in the last 7 days: After two weekly collections
- Tracked since: Jul 10, 2026

[All IQVIA jobs](https://jobs.opennash.com/companies/iqvia/) · [Weekly hiring report](/reports/hiring/)

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