Clinical Research Associate I & II - Site Management SPAIN

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

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 selection of 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.’

This role is working in our core clinical site management function. The team works with multiple sponsors across a multitude of therapy areas and phases giving you the opportunity to improve and develop your experience. With strategic site relationship managers supporting you throughout your role this is a fantastic opportunity for you to embed yourself in the wider clinical operations team and work on ground-breaking new medicine development.

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
• If appropriate, co-monitoring, training and mentoring of junior members in the team

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:

• We offer genuine career development opportunities for those who want to grow as part of the organisation
• The chance to work on cutting edge medicines right at the forefront of new medicines development
• IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
• As a CRA you will receive an iPad and use of key developments such as site visit app’s, site visit report app’s that allow CRA’s to do their day job more efficiently.
• Flexible conditions and an attractive remuneration package
• Location flexibility: you can work either from our Madrid or Barcelona office or remotely from home (different locations in Spain)

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.