Clinical Research Associate
2 settimane fa
Job Overview
Clinical Research Associates at IQVIA play a crucial role in the successful execution of clinical trials. As a Clinical Research Associate - Site Management, you will be responsible for engaging in structured training programs to gain knowledge and skills required to independently conduct clinical monitoring visits.
Key Responsibilities
- Complete therapeutic, protocol, and clinical research training to perform job duties.
- Gain experience in study procedures by working with experienced clinical staff.
- Under close supervision, perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and good clinical practices.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution.
- Collaborate and liaise with study team members for project execution support as appropriate.
Qualifications
- Bachelor's Degree in a scientific discipline or healthcare preferred.
- Equivalent combination of education, training, and experience may be accepted in lieu of degree.
- Computer skills including proficiency in the use of Microsoft Word, Excel, and PowerPoint.
- Written and verbal communication skills, including good command of the English language.
- Organizational and problem-solving skills.
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