Senior Clinical Research Associate 1 - Sponsor dedicated

IQVIA; Madrid; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A leading clinical research organization is seeking a Senior Clinical Research Associate to perform site monitoring and ensure compliance with regulatory standards. This role requires a degree in a scientific discipline, at least 2 years of monitoring experience, and proficiency in Spanish and English. The successful candidate will enjoy a supportive work environment with opportunities for career growth and benefits.

Servicios

Resources that promote career growth

Flexible work schedules

Mobile phone

Attractive benefits package

Formación

• At least 2 years of on‑site monitoring experience is required.
• Good knowledge of clinical research regulatory requirements is necessary.
• Excellent command of Spanish and English language skills are needed.

Responsabilidades

• 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.

Conocimientos

On-site monitoring experience

Knowledge of clinical research regulatory requirements

Excellent command of Spanish and English

Good computer skills including MS Office

Organizational skills

Time-management skills

Problem-solving skills

Flexibility to travel

Driver’s license class B

Educación

University degree in scientific discipline or health care

Descripción del empleo

Senior Clinical Research Associate 1

IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.

When you join IQVIA Spain as a sponsor‑dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.

With access to world‑class training and mentoring, you’ll 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.

Responsibilities

• 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 (GCP) and International Conference on Harmonization (ICH) guidelines
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
• Collaborating with experts at study sites and with client representatives

Qualifications

• University degree in scientific discipline or health care
• At least 2 years of on‑site monitoring experience
• Good knowledge of clinical research regulatory requirements
• 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
• Better Work‑Life balance, optimal DOS
• 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.