Description
We are seeking a Clinical Research Coordinator to support our clinical research team in Columbus, Ohio.
The successful candidate will assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams with maintaining clinical documents and systems, preparing and handling clinical documentation and reports, and tracking clinical trial supplies.
Key responsibilities include:
- Assisting CRAs and RSU teams with updating and maintaining clinical documents and systems
- Preparing, handling, distributing, filing, and archiving clinical documentation and reports
- Reviewing study files for completeness
- Assisting with tracking and management of Case Report Forms (CRFs), queries, and clinical data flow
- Acting as a central contact for the clinical team for designated project communications and correspondence
- Accompanying CRAs on site visits to assist with clinical monitoring duties upon completion of required training
Requirements:
- Bachelor's degree
- 3 years of administrative support experience
- Computer skills including Microsoft Word, Excel, and PowerPoint
- Good command of English language
- Effective time management and organisational skills
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
- Awareness of applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
We offer a competitive salary ranging from $35,800 to $123,000 per year, depending on experience and qualifications.
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