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 vital role in ensuring the success of clinical trials by providing administrative support to the Clinical Research Associates and Regulatory and Start-Up teams. Your primary responsibility will be to maintain the Trial Master File, ensuring that all clinical documents and systems are up-to-date and accurate.

Key Responsibilities

• Collaborate with CRAs and RSU team members to update and maintain clinical documents and systems, ensuring compliance and performance within project timelines.

• Assist the clinical team in preparing, handling, distributing, filing, and archiving clinical documentation and reports according to standard operating procedures.

• Conduct periodic reviews of study files to ensure completeness.

• Support CRAs and RSU with the preparation, handling, and distribution of Clinical Trial Supplies and maintenance of tracking information.

• Assist with the tracking and management of Case Report Forms (CRFs), queries, and clinical data flow.

• Serve as a central point of contact for the clinical team for designated project communications, correspondence, and associated documentation.

• May accompany CRAs 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.

• Equivalent combination of education, training, 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.

• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

• Familiarity with clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

• Knowledge of applicable protocol requirements.

About IQVIA

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



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