Clinical Research Associate 1 - CFSP

IQVIA; Barcelona; Presencial; EUR 25.000 - 35.000; Jornada completa

Descripción de la vacante

A leading global provider of clinical research services is seeking a Clinical Research Associate in Barcelona. The role involves site selection, monitoring clinical trials, and ensuring regulatory compliance. Ideal candidates will have a university degree in a scientific discipline and at least 6 months of experience in the Pharma industry. Fluency in Spanish and English is required. The organization promotes career growth and offers a flexible working environment.

Servicios

Resources that promote your career growth

Support for flexible work schedules

Programs to build therapeutic knowledge

Excellent working environment

Mobile phone and attractive benefits package

Formación

• University degree in scientific discipline or health care.
• At least 6 months of experience in Pharma Industry or Clinical Trials.
• Very good computer skills including MS Office.
• Excellent command of Spanish and English language.

Responsabilidades

• Perform site selection, initiation, monitoring and close‑out visits.
• Support the development of a subject recruitment plan.
• Evaluate the quality and integrity of site practices in accordance with regulatory requirements.
• Manage progress by tracking regulatory submissions and data query resolutions.
• Collaborate with experts at study sites and with client representatives.

Conocimientos

Excellent command of Spanish

Excellent command of English

Organizational skills

Time management skills

Problem-solving skills

Very good computer skills including MS Office

Ability to establish and maintain effective working relationships

Flexibility to travel

Driver's license class B

Educación

University degree in scientific discipline or health care

Descripción del empleo

Clinical Research Associate

Your responsibilities will include:

• Performing site selection, initiation, monitoring and close‑out visits after completing training period
• Supporting the development of a subject recruitment plan
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
• Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
• Collaborating with experts at study sites and with client representatives

Qualifications:

• University degree in scientific discipline or health care
• At least 6 months of experience in Pharma Industry, and/or Clinical Trials environment
• Very good computer skills including MS Office
• Excellent command of Spanish and English language
• Organizational, time management and problem‑solving skills
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Flexibility to travel
• Driver’s license class B

What you can expect:

• Resources that promote your career growth
• Leaders that support flexible work schedules
• Programs to help you build your therapeutic knowledge
• Excellent working environment in a stable, international, reputable company
• Mobile phone and attractive benefits package

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.

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.