Clinical Research Associate managing clinical trials for Summit Therapeutics. Supporting complex global studies while ensuring adherence to metrics and quality deliverables from study planning to close out.
Responsibilities
Supports all aspects of Clinical Trial Management for complex, global studies
Collaborates with functional team members, CROs, and vendors
Directs and completes communication between the project team and site personnel
Reviews, approves, and tracks vendor invoices and manages accruals and payment process for all assigned clinical trial vendors
Initiates and builds professional relationships with clinical site staff
Responsible for the development and management of clinical trial documents
Provides close oversight on findings on the monitoring reports
Requirements
Bachelor's degree or equivalent in life science, nursing, pharmacy, medical laboratory technology, or related field preferred
3+ years of clinical research experience in conducting clinical trials
Prior phase II or III experience required
Sophisticated understanding and highly skilled utilization of Microsoft Apps such as Outlook, Word, Excel, and Teams
Ability to travel internationally to visit clinical sites and for study meetings (up to 20%)
Excellent interpersonal and decision-making skills
Experience in working in a small organization a plus
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