Clinical Research Associate 2 - CFSP

IQVIA; Madrid; Presencial; EUR 30.000 - 40.000; Jornada completa

Descripción de la vacante

Join a leading clinical research organization as a Junior Clinical Research Associate. You will be part of a dedicated team responsible for site oversight, ensuring compliance with regulations, and managing study progress, all while gaining invaluable experience in a reputable environment. This role offers a unique opportunity to grow your career in the clinical research field while working with a diverse and innovative team.

Servicios

Career growth resources

Flexible work schedules

Programs to build therapeutic knowledge

Mobile phone

Attractive benefits package

Formación

• University degree in scientific discipline or health care required.
• Experience in Pharma Industry or Clinical Trials environment preferred.
• Excellent command of Spanish and English languages.

Responsabilidades

• Performing site selection, initiation, monitoring, and close-out visits.
• Supporting development of subject recruitment plans.
• Evaluating quality and integrity of site practices.

Conocimientos

Computer skills

Organizational skills

Time management

Problem-solving skills

Interpersonal skills

Flexibility to travel

Educación

University degree in scientific discipline 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 junior 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 representatives

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.

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.