Freelance CRA - Spain

IQVIA LLC; Barcelona; Presencial; EUR 32.000 - 42.000; A tiempo parcial

Descripción de la vacante

IQVIA is seeking two Freelance CRAs to support Phase III studies across Spain, with ~0.5 FTE per assignment (18 hours/week). Responsibilities include IMVs, ensuring protocol adherence, and data verification. Travel within Spain is required and start is ASAP for an initial ~6 months.

Ideal candidates will have at least 2 years of CRA monitoring experience, Phase III trial exposure, and fluency in Spanish and English. Ability to work independently and strong organizational skills are essential.

Formación

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

Responsabilidades

• 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

Conocimientos

CRA monitoring

Phase III experience

ICH-GCP knowledge

Independent work

Communication skills

Spanish & English

Descripción del empleo

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

#LI-DNP #LI-CES #LI-HCPN #LI-XS

Company Information

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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.