Remote Visit Coordinator, US Regional Specialist
New
I
IQVIAClinical Research
Home-based in USAFull-TimeMiddle
Salary51,000 - 127,400 USD per year
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Job Details
- Languages
- English
- Experience
- Two (2) years research experience strongly preferred.
- Required Skills
- GCPMS OfficeHIPAAData management
Requirements
- Bachelor's degree (B. A. / B. S.) or equivalent combination of education, training, and experience.
- Two (2) years research experience strongly preferred.
- Strong written and verbal communication skills with a good command of English.
- Strong presentation skills.
- Strong problem-solving skills and ability to make informed decisions.
- Excellent computer skills, proficient in MS Word, Excel, and PowerPoint.
- Ability to obtain knowledge and master all clinical trial database systems.
- Proven ability to coordinate multiple studies adhering to regulatory and institutional guidelines.
- Excellent organizational skills with attention to detail and ability to handle multiple tasks.
- Ability to perform under pressure while prioritizing multiple projects.
- Knowledge of FDA Good Clinical Practices (GCP), FDA regulations, and SOPs.
Responsibilities
- Conduct outreach and training for investigator sites opting into RRC services.
- Train and onboard research clinicians, ensuring they are prepared and study-ready.
- Manage access to systems like Study Hub and Thinking Cap for site staff and clinicians.
- Receive and process Visit Request Forms (VRFs) and assign clinicians for remote visits.
- Coordinate visit logistics including supplies, equipment, and courier services.
- Ensure all required documentation is complete, accurate, and uploaded.
- Maintain and update Smartsheet trackers for sites, visits, and clinicians.
- Perform quality checks on source documents and ensure timely corrections.
- Ensure compliance with GCP, ICH, HIPAA, and IQVIA SOPs.
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