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Clinical Research Coordinator
2 weeks ago
Clinical Trial Assistants play a crucial role in ensuring the smooth operation of clinical trials. As a member of our team, you will be responsible for providing administrative support to our Clinical Research Associates and Regulatory and Start-Up teams.
Key Responsibilities:
- Assist with updating and maintaining clinical documents and systems that track site compliance and performance within project timelines.
- Prepare, handle, distribute, file, and archive clinical documentation and reports according to the scope of work and standard operating procedures.
- Review study files for completeness and assist with periodic review.
- Coordinate the tracking and management of Case Report Forms (CRFs), queries, and clinical data flow.
Qualifications:
- High School Diploma or equivalent required.
- 3-4 years of administrative support experience preferred.
- Minimum one year of clinical research experience is highly desirable.
- Strong computer skills including Microsoft Word, Excel, and PowerPoint are essential.
- Excellent written and verbal communication skills are required.
About Us:
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.
