
Clinical Project Administrator
4 days ago
Clinical Trials Coordinator Role
IQVIA is seeking a skilled Clinical Trials Coordinator to join our Functional Service Partnerships Team.
The successful candidate will provide administrative support to clinical projects, updating clinical systems and databases, and assisting with general administrative functions as required.
Key Responsibilities:
- Assist in accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.
- Prepare, handle, distribute, file, and archive clinical documentation and reports according to standard operating procedures.
- Manage Case Report Forms (CRFs), queries, and clinical data flow.
- Serve as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.
- Accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and approval.
Requirements:
- Awareness of applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Knowledge of protocol requirements as provided in company training.
- Computer skills, including working knowledge of Microsoft Word, Excel, and PowerPoint.
- Excellent written and verbal communication skills, including proficiency in the English language.
- Effective time management and organizational skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
- High school diploma or equivalent and 3 years of administrative support experience, or an equivalent combination of education, training, and experience.
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