Senior Clinical Operations Coordinator
hace 4 semanas
The role of the Senior Study Support Assistant at ICON plc is a critical position that requires a high level of expertise in clinical trial operations. The successful candidate will be responsible for supporting the Study Start-up Associate with various tasks, including tracking, filling, collating, and verifying submission documentation for regulatory authorities.
Key Responsibilities:- Tracking and monitoring submission progress, updating relevant tracking systems, and ensuring timely submission of documents to regulatory authorities.
- Coordinating and maintaining departmental electronic filing systems, setting up and ensuring the accuracy of electronic documentation.
- Attending meetings as requested, preparing and presenting slides, and assisting in the production of reports and documents.
- Assisting in the coordination of payments to regulatory authorities and being familiar with ICH GCP and ICON SOPs.
- A high school diploma or local equivalent with good interpersonal skills and attention to detail.
- Excellent written and verbal communication skills in English.
- Research or healthcare-related academic or work experience is preferable but not essential.
ICON plc is committed to providing a workplace free of discrimination and harassment. We offer a range of benefits, including competitive salaries, annual bonuses, health-related benefits, and retirement plans. We are an equal opportunity employer and welcome applications from diverse candidates.
We encourage applicants to apply, regardless of whether they meet all the requirements. If you are a current ICON employee, please click here to apply.
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