cra 1

hace 2 semanas


Barcelona, Barcelona, España IQVIA A tiempo completo

Join us in our exciting journey

We currently require a motivated, creative and enthusiastic professional specializing in clinical trials to join our rapidly growing Site Management division.

As an experienced Clinical Research Associate, you might be eager to broaden your therapeutic, geographic, or study exposure. Or maybe you are eyeing a future beyond monitoring with our development opportunities. At IQVIA, you'll receive training and development to plan and advance your career in the direction you desire; we do not believe in a 'career ceiling.'

This position involves working in our core clinical site management function. The team collaborates with multiple sponsors across a variety of therapy areas and phases, providing you with the chance to enhance and grow your expertise. With strategic site relationship managers backing you throughout your role, this is an excellent opportunity for you to immerse yourself in the broader clinical operations team and contribute to revolutionary new medicine development.

Our clients are pharmaceutical companies committed and enthusiastic about enhancing the lives of patients across various therapeutic areas.

The role: Responsibilities

  • Perform site selection, initiation, monitoring, and close-out visits and collaborate with sites to adjust, drive, and monitor subject recruitment plans.
  • Administer protocol and related study training to designated sites and establish regular lines of communication.
  • Evaluate the quality and integrity of study site practices concerning the proper conduct of the protocol and adherence to relevant regulations – escalating quality concerns when necessary.
  • Oversee the progress of assigned studies by monitoring regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
  • Create and maintain proper documentation regarding site management, monitoring visit findings, and action plans.
  • If suitable, participate in co-monitoring, training, and mentoring junior team members.

Our ideal candidate: Skills & other requirements

  • In-depth knowledge and proficiency in applying applicable clinical research regulatory requirements; e.g., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Thorough therapeutic and protocol knowledge as provided in company training
  • Exceptional organizational and problem-solving capabilities
  • Effective time management abilities
  • Strong written and verbal communication skills, including a good command of English and Spanish
  • Bachelor's degree in a health care or other scientific discipline or equivalent education
  • Minimum 1 year of independent on-site monitoring experience

What we offer:

  • We provide genuine career development opportunities for those aiming to evolve within the organization.
  • The opportunity to work on cutting-edge medicines at the forefront of new medicine development.
  • Access to substantial data pools at IQVIA, enabling better site selection and recruitment, thus enhancing the productivity of CRAs and making site discussions more fruitful. Next-generation clinical development.
  • As a CRA, you will be equipped with an iPad and access to key developments like site visit apps and site visit report apps that facilitate the efficiency of CRA responsibilities.
  • Flexible conditions and an appealing remuneration package.
  • Location flexibility: work from either our Madrid or Barcelona office or remotely from home (various locations in Spain)

We invite you to join IQVIATM

  • Ranked by Great Place to Work as the second-best company to work for in Spain (March 2019)
  • FORTUNE Magazine's World's Most Admired Companies list for the third consecutive year (January 2020)
  • Recipient of the 2016 Scrip Awards for Best Full-service Provider Contract Research Organization (CRO)
  • Winner of the 2016 Eagle Award from the Society for Clinical Research Sites (SCRS) for the fourth straight year.
  • Received a site-nominated award acknowledging contract research organizations (CROs) and biopharmaceutical sponsors committed to fostering positive relationships with research sites through leadership, professionalism, and integrity.
  • IQVIATM named in The International Association of Outsourcing Professionals (IAOP) 2017 Global Outsourcing 100 List, recognizing top service providers across various industries worldwide.

IQVIATM is an equal opportunity employer. We base our employment decisions on qualifications and merit, strictly prohibiting discrimination based on any unlawful factors such as age, race, national origin, gender, or other status.

We acknowledge that achieving significant outcomes necessitates not just the right strategy but also the right people. Regardless of your position, we encourage you to reshape healthcare with us. You will play a vital role in assisting our clients in advancing healthcare, and no matter your career aspirations, we are here to support your journey.

IQVIA is a prominent global provider of advanced analytics, technology solutions, and clinical research services to the life sciences sector. We advocate for pushing the boundaries of human science and data science to maximize our impact – aiding our clients in creating a healthier world. Learn more at


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