Peluquero Freelance

Peluquería Montull

Barcelona

On-site

EUR 25,000 - 40,000

Part time

11 days ago

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

IQVIA is seeking Freelance CRAs to support two Phase III studies across Spain. The role is approximately 0.5 FTE (18 hours per week) with travel to sites, starting ASAP and lasting about six months. You will monitor sites, ensure protocol adherence, and support investigators.

Fluency in Spanish and English is required, with strong ICH-GCP knowledge and independent working ability. Expect 2-3 site visits per month across roughly 10 sites in Spain.

Qualifications

  • 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.

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.

Skills

CRA monitoring
Phase III experience
ICH-GCP
Communication skills
Organizational skills
Spanish & English fluent

Job description

Barcelona, Spain
Madrid, Spain
Part time
R
Join IQVIA Biotech as a Freelance CRA supporting two Phase III clinical studies in 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


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.


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.


EEO Minorities/Females/Protected Veterans/Disabled

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Freelance CRA - Spain
Freelance CRA - Spain

IQVIA • Barcelona

On-site
EUR 29,000 - 45,000
Freelance CRA - Spain
Freelance CRA - Spain

IQVIA • Madrid

On-site
EUR 26,000 - 36,000
Clinical Research Associate 2 - Multi-Sponsor - Based in Madrid/Barcelona
Clinical Research Associate 2 - Multi-Sponsor - Based in Madrid/Barcelona

Iqvia • Madrid

On-site
EUR 52,000 - 72,000
Mobile phone
Attractive benefits package
Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona
Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona

IQVIA • Barcelona

On-site
EUR 36,000 - 48,000
Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona
Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona

IQVIA • Madrid

On-site
EUR 37,000 - 52,000
Career growth
Flexible schedule
Therapeutic knowledge
+1
Senior Clinical Research Associate 1 - Sponsor dedicated
Senior Clinical Research Associate 1 - Sponsor dedicated

IQVIA • Barcelona

On-site
EUR 42,000 - 64,000
Mobile phone included
Excellent benefits package
Clinical Research Associate 2 - CFSP
Clinical Research Associate 2 - CFSP

IQVIA • Barcelona

On-site
EUR 42,000 - 54,000
Career growth resources
Flexible work schedules
Therapeutic knowledge programs
+2
Clinical Research Associate 2 - CFSP
Clinical Research Associate 2 - CFSP

IQVIA • Madrid

On-site
EUR 32,000 - 46,000
Career growth resources
Flexible work schedules
Therapeutic knowledge programs
+2
Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona
Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona

IQVIA • Barcelona

Hybrid
EUR 32,000 - 42,000
Mobile phone
Benefits package
Senior Clinical Research Associate 1 - Sponsor dedicated
Senior Clinical Research Associate 1 - Sponsor dedicated

IQVIA • Madrid

On-site
EUR 42,000 - 62,000