Descripción de la oferta
Descripción del trabajo
Join us in our exciting journey!!
We currently require a motivated, creative and enthusiastic clinical trials professional to join our rapidly growing Site Management 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 Associates 2 to work Full Services model to work with 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.
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.
Qualifications
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.
2‑4 years of independent on‑site monitoring experience.
Benefits
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!
Why 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 (January 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 on 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.
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!
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.
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.
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