Freelance CRA - Spain

IQVIA; United States; Remote; USD 57,000 - 83,000; Part time

Job summary

IQVIA Biotech is seeking two Freelance CRAs to monitor Phase III studies across Spain, each at ~0.5 FTE (18 hours/week). Travel to approximately 10 sites is expected, with 2-3 visits per month. Start ASAP for an initial ~6 months.

Fluency in Spanish and English required; independent work style essential. Responsibilities include IMVs, ensuring protocol adherence, data verification, and supporting investigators.

Qualifications

• Minimum 2 years of CRA monitoring experience.
• Experience on Phase III clinical trials is required.
• Strong knowledge of ICH-GCP and trial processes.
• Ability to work independently with minimal supervision.
• Willingness to travel within Spain and across sites.

Responsibilities

• Perform Interim Monitoring Visits at clinical trial sites.
• Ensure protocol adherence and ICH-GCP compliance.
• Verify source documents and study data accuracy.
• Support investigators and site personnel as needed.
• Identify site issues and implement action plans.
• Collaborate with project teams to ensure study delivery.

Skills

CRA monitoring

Phase III experience

ICH-GCP

Independent work

Travel within Spain

Spanish fluent

English fluent

Communication

Organization

Job description

Join IQVIA Biotech as a Freelance CRA supporting two Phase III clinical studies in Spain.

We are currently looking for two experienced CRAs , each supporting approximately 0.5 FTE (18 hours/week), with the possibility of combining assignments depending on availability and project needs. The role focuses primarily on monitoring activities across sites throughout Spain.

Key Details

• Location: Spain (nationwide travel)
• Openings: 2 Freelance CRA positions
• FTE: Approximately 0.5 FTE per assignment (18 hours/week)
• Start: ASAP
• Duration: Approximately 6 months
• Travel: Around 2-3 site visits per month
• Sites: Approximately 10 sites across Spain

Responsibilities

• Perform Interim Monitoring Visits (IMVs) at clinical trial sites
• Ensure protocol adherence and ICH-GCP compliance
• Verify source documents and study data
• Support investigators and site personnel
• Identify and follow up on site issues and action plans
• Collaborate with project teams to ensure successful study delivery

Requirements

• Minimum 2 years of CRA monitoring experience
• Previous Phase III clinical trial experience
• Strong knowledge of ICH-GCP and clinical trial processes
• Ability to work independently
• Excellent communication and organizational skills
• Fluent Spanish and English
• Willingness to travel within Spain

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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.