Clinical Research Associate 2 - CFSP

IQVIA; Barcelona; Presencial; EUR 42.000 - 54.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Career growth resources

Flexible work schedules

Therapeutic knowledge programs

Stable international company

Mobile phone

Descripción de la vacante

IQVIA Spain is seeking a Clinical Research Associate to join our Sponsor dedicated team in Barcelona. The CRA will conduct site visits, support recruitment plans, and ensure regulatory compliance across therapeutic areas.

The role requires travel, English/Spanish fluency, and a background in pharma or clinical trials, with strong MS Office skills and organizational abilities.

Formación

• University degree in scientific discipline or health care.
• Experience in Pharma Industry or Clinical Trials environment.
• Excellent command of Spanish and English.
• Strong organizational, time management and problem-solving skills.
• Ability to travel and hold a valid driver's license (Class B).

Responsabilidades

• Perform site selection, initiation, monitoring and close-out visits.
• Support the development of a subject recruitment plan.
• Evaluate site practices for compliance with GCP/ICH.
• Track regulatory submissions, recruitment, CRF completion and data queries.
• Collaborate with study sites and client representatives.

Conocimientos

Spanish language

English language

MS Office

Organizational skills

Time management

Problem solving

Driving license

Educación

University degree in life sciences or health care

Herramientas

MS Office

Descripción del empleo

Clinical Research Associate

IQVIA Spain is looking for talented and motivated team member to join our Sponsor dedicated team as CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.

Your Responsibilities Will Include

• Performing site selection, initiation, monitoring and close-out visits


• 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 representations

Qualifications

• University degree in scientific discipline or health care


• 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 stabile, 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. 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.