Clinical Trial Assistant

• Join us in our exciting journey!!

We are currently looking for a motivated, creative and enthusiastic clinical trials professional to join our FSP division. This role is to work dedicated to one of our main pharmaceutical clients. With a fantastic work/life balance, this is a great opportunity for a Clinical Trials Assistant willing to discover what means to work in one of the best CROs worldwide! A career with IQVIA connects you to great opportunity to achieve professional success and impact healthcare around the world.

The role: Responsibilities

Provide administrative support to clinical projects and update clinical systems and databases. Assists with general administrative functions, as required, in support of designated clinical team members.

• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.
• Collaborate on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files and completeness.
• Collaborate on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
• Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
• Assist in training and orienting new staff. May act as a mentor for less experienced CTAs.
• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.
• Perform assigned administrative tasks to support team members with clinical trial execution.

Our ideal candidate: Skills & other requirements

• Basic knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Knowledge of applicable protocol requirements as provided in company training
• Previous experience within a clinical trials environment is required.
• Previous experience with regulatory submissions to EC and competent authorities is mandatory.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
• Effective written and verbal communication skills
• Effective time management and organizational skills
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
• Good command of English language.

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 fourth year in a row (January 2021)
• 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?

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 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at .

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. 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. Learn more at

Fecha de publicación: 09/06/2022