IQVIA
Healthcare
ClinicalResearchAssociate
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Clinical Research Associate at IQVIA. Skills: Site monitoring, Clinical research, Regulatory requirements. Perform site selection visits. Perform site initiation visits”
Industry & Context.
Data query resolution
Frequent travel to sites
What They're Looking For.
Must Have
1 year of on-site monitoring experience, Fluent command of English and Serbian language, Valid driver´s license
Nice to Have
Bachelor's degree in a health care, MD or Pharmacist
What You'll Do.
Perform site selection visits
Perform site initiation visits
Perform site monitoring visits
Perform site close-out visits
Maintain appropriate documentation
Support development of subject recruitment plan
Establish regular lines of communication
Administer protocol training to assigned sites
Administer study training to assigned sites
Evaluate quality of site practices
Evaluate integrity of site practices
Escalate quality issues as appropriate
Manage progress by tracking regulatory submissions
Manage progress by tracking recruitment
Manage progress by tracking CRF completion
Manage progress by tracking data query resolution
How You'll Work.
Team & Collaboration
Collaborating with colleagues; Communicating with customers
Communication Scope
Written communication; Verbal communication
Full Job Description
**If you are looking to upgrade your CRA career, this is your chance to connect with us and explore opportunities within a leading global CRO!** **_While projects vary, your typical CRA responsibilities will include_** * 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 ** _You should have_** * 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](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 mater
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