Join us in our exciting journey!!
A career with IQVIA connects you to great opportunities to achieve professional success and impacts healthcare around the world. As Clinical Research Associate in this team, you will be part of our single sponsor outsourced function dedicated to one of our key pharmaceutical clients.
Join us and benefit from our advantages!!
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
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
Required Knowledge and skills:
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
Previous experience working with oncology or cardiovascular clinical trials
In depth therapeutic and protocol knowledge as provided in company training
Strong written and verbal communication skills including good command of English language
Excellent organizational and problem-solving skills
Effective time management skills
Minimum Required Education & Experience :
A Bachelor’s degree in a health care or other scientific discipline or educational equivalent
Minimum 1.5 years of monitoring experience as an independent CRA
Whatever your career goals, we are here to ensure you get there!
We invite you to join IQVIA™.
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