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Clinical Research Associate 1 & 2, Sponsor-Dedicated, Spain

Location: Spain; Barcelona, Spain
R1190064

When you join IQVIA 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. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development.

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.

  • Full Time
  • Level: Entry-level, Mid-level, Senior-level
  • Travel: Yes

Success profile

What makes sponsor-dedicated CRAs at IQVIA successful? Check out the top traits we’re looking for and see if you have the right mix.

  • COLLABORATIVE
  • DETAIL-ORIENTED
  • COMMUNICATOR
  • INDEPENDENT
  • CURIOUS
  • PROBLEM-SOLVER

Explore this
career path

As you grow your CRA career at IQVIA, you’ll play an important role in helping our customers drive healthcare forward and impact the lives of patients around the world.

Quote

Alberto

IQVIA offers a robust development plan for CRAs, including trainings, mentorship programs, and cross-functional career meetings. These conditions made me feel ready, confident and well-trained to execute the role of a CRA with quality and integrity.

Alberto, Clinical Research Associate 2
Oliver

IQVIA places real emphasis on the training and development of employees. This is invaluable for someone starting out or looking to progress their career in clinical research. I find it extremely rewarding to work for a company that strives to grow and retain its talent and equips you with the skills and experience needed to succeed in your career.

Oliver, Clinical Research Associate 1

What you
can expect

  • Professional Development

    Resources that promote your career growth

  • Work-Life Balance

    Leaders that support flexible work schedules

  • Growth Potential

    Clear pathways to success

  • Collaboration

    Teams that work together to achieve common goals

  • Variety

    Dynamic work environments that expose you to new experiences

  • Best-in-class Training

    Programs to help you build knowledge and gain skills

Clinical Research Associate 1 & 2, Sponsor-Dedicated, Spain

Apply now
Location: Madrid, Madrid, Spain R1190064 Posted: 10/11/2021

Job description

Join us in our exciting journey!!

We currently require a motivated, passionate and enthusiastic clinical trials professional to join our rapidly growing Clinical Functional Service Partnership (CFSP) division.

As an experienced Clinical Research Associate, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond monitoring with our development opportunities. At IQVIA, you’ll have training and development to plan and progress your career in the direction you choose; we do not believe in a ‘career ceiling.’

IQVIA is expanding in Spain - we currently have multiple exciting vacancies for Clinical Research Associate's to work sponsor-dedicatedto one of our key pharmaceutical clients. If you have independent site monitoring experience as CRA and want to discover how a true partnership between the CRO and sponsor works, then this is the right opportunity for you!

Our clients are pharmaceutical companies who are dedicated and passionate about improving the lives of patients across several therapeutic areas.

The role: Responsibilities

  • Perform site selection, initiation, monitoring and close-out visits and work with sites to adapt, drive and track subject recruitment plans.
  • Administer protocol and related study training to assigned sites and establish regular lines of communication.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations  – escalating quality issues as appropriate.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans

Our ideal candidate: Skills & other requirements

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

What we offer:

  • Working with one of the TOP 5 sponsors globally on international projects.
  • Focus on quality, not quantity! We invest in keeping our teams stable, so workload is consistent.
  • The chance to work on cutting edge medicines right at the forefront of drug development.
  • Genuine career development opportunities for those who want to grow as part of the organization.
  • Flexible conditions and an attractive remuneration package.
  • Office or home-based roles available! 

We invite you to join IQVIA™

  • Recognized 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 year in a row (June 2020)
  • Recognized by the 2016 Scrip Awards as the Best Full-service Provider Contract Research Organization (CRO)
  • Awarded the 2016 Eagle Award from the Society for Clinical Research Sites (SCRS) for the fourth consecutive year.
  • A site-nominated award recognizing contract research organizations (CRO) and biopharmaceutical sponsors dedicated to building positive relationships with research sites through leadership, professionalism and integrity.
  • IQVIA™ named in The International Association of Outsourcing Professionals (IAOP) 2017 Global Outsourcing 100® List which recognizes the world’s best service providers across a range of industries.

IQVIA™ is an equal opportunity employer. We make employment decisions based on qualifications and merit. We prohibit discrimination based on any unlawful consideration such as age, race, national origin, gender or other "protected status.“

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and whatever your career goals, we are here to ensure you get there!

Are you interested or do you know the ideal candidate?

  • If you know the right candidate or for more information on this role please contact susana.cangas@iqvia.com or ana.rey@iqvia.com
  • Please note is necessary that your application is registered in our Talent Network to process your candidacy

#CRASDAJD

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

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