Research Project Coordinator
4 days ago
ICON Clinical Research Limited is committed to providing a workplace free of discrimination and harassment.
As a Project Manager Laboratory, you will be responsible for ensuring client satisfaction by acting as the Client's main contact in all matters regarding ICON Central Laboratories' (ICL) services, including the setup and day-to-day management of studies.
Key responsibilities include:
- Acting as the sponsor's main contact person in all matters regarding our central laboratory services.
- Following up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives, and the ICON Site Services Department.
- Reviewing newly assigned protocols and Amendments.
- Coordinating the completion of the Clinical Laboratory Worksheet (CLW) and communicating information as required to other departments within ICON Laboratories (and ICON Clinical CRO if appropriate).
- Developing and maintaining project management documents, including project timelines, project management plans, communication plans, and risk assessment plans.
- Maintaining study-specific study files and ensuring that all appropriate documents are maintained.
What you need:
Prior relevant experience working in a clinical laboratory, clinical trials, project management, or customer management/account management role in a life sciences-related organization is preferable.
Bachelor's degree or local equivalent in Science, Business, or related field or local equivalent. An alternative combination of experience, education, and training determined by management to be equivalent to the foregoing.
We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term career.
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