Clinical Research Coordinator
2 days ago
Toledo
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.
