Clinical Research Coordinator
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Clinical Research Coordinator in Toledo
Working Hours: 20- 24 hours per week
Start Date : Immediately
Duration : Approximately 6 months
IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Toledo. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.
Key Responsibilities
As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including:
- Prescreening and Screening tasks
- Review charts from the site data base
- Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems
- Supporting patient screening and enrollment, including handling informed consent and privacy documentation
- Coordinating logistical activities for study procedures in line with the study protocol
- Processing lab samples
- Attend patient visits including ECG, vitals and potentially blood draws
- Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness
- Patient education
- Communicating with study monitors and responding to study-related inquiries
- Carrying out general administrative tasks related to the study
Your Profile
We are looking for candidates who bring a combination of education, experience, and skills:
- Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)
- Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
- Good knowledge of medical terminology
- Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
- Must have at least 2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
- Excellent interpersonal and communication skills
- Strong organizational skills and attention to detail
- Fluency in English
Why Join IQVIA?
At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference.
Interested?
If this sounds like the right opportunity for you, we encourage you to apply today.
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