Clinical Research Associate - Multi-Sponsored Model

• →Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
• →Supporting the development of a subject recruitment plan
• →Establishing regular lines of communication plus administering protocol and related study training to assigned sites
• →Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
• →Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution 

• A Bachelor's degree in a health care, MD or Pharmacist preferred.
• At least 1 year of on-site monitoring experience.
• Good written and verbal communication skills including fluent command of English and Serbian language.
• A valid driver´s license as the role requires frequent travel to sites.
• You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You also have a good knowledge of applicable clinical research regulatory requirements.

Apply now and let´s connect for current and/or future opportunities!

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.