Clinical Research Coordinator

3 weeks ago


Solna Municipality, Sweden IQVIA Full time

Job Overview
As a Clinical Trial Assistant at IQVIA, you will play a crucial role in ensuring the smooth execution of clinical trials. Your primary responsibility will be to assist the Clinical Research Associates and Regulatory and Start-Up teams in maintaining accurate and complete Trial Master Files. This involves working closely with the team to update and maintain clinical documents and systems, ensuring compliance and performance within project timelines.

Key Responsibilities
Assist in the preparation, handling, and distribution of clinical documentation and reports, adhering to standard operating procedures.
Collaborate with the clinical team to review study files for completeness and accuracy.
Provide support in the tracking and management of Case Report Forms, queries, and clinical data flow.
Serve as a central contact for the clinical team, handling project communications, correspondence, and associated documentation.
May accompany Clinical Research Associates on site visits to assist with clinical monitoring duties, upon completion of required training.

Requirements
High School Diploma or equivalent.
3 years of administrative support experience, or equivalent combination of education and experience.
Proficiency in Microsoft Office, including Word, Excel, and PowerPoint.
Excellent written and verbal communication skills, with fluency in English and local language.
Strong time management and organizational skills, with the ability to establish and maintain effective working relationships.

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We strive to push the boundaries of human science and data science to create a healthier world. Learn more at https://www.iqvia.com/.



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