Join us in our exciting journey!!
A career with IQVIA connects you to great opportunity to achieve professional success and impact healthcare around the world.
This role is working in our single sponsor outsourced function dedicated to our key pharmaceutical client . With a fantastic work / life balance, this is a great opportunity for a Clinical Research Associate willing to to discover how a true partnership between the CRO and sponsor works! Join us and benefit from its advantages
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
Strong written and verbal communication skills including good command of English and Portuguese.
Excellent organizational and problem-solving skills
Effective time management skills
Bachelor's degree in a health care or other scientific discipline or educational equivalent
Mínimum 2 years 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
Excellent salary and benefits package
Flexible working hours
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 marta.saiz iqvia.com
Please note is necessary that your application is registered in our Talent Network to process your candidacy