Sr CRA or CRA II - sponsor dedicated - PORTUGAL (R1114012) - Lisboa, Portugal - IQVIA™

Date de publication 2/21/2020

Résumé de l'offre

  • Type d'employé
    CDI / CNE
  • Expérience
    Not Specified
  • Date de publication
    2/21/2020
  • Job ID:
    R1114012

Description de l'offre

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.

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 grear 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  

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

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
  • Gnuine career development opportunities for those who want to grow as part of the organization
  • Excellent salary and benefits package
  • Flexible working hours

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.



Job ID: R1114012