Kim Cotten-West
Sr. Clinical Trial Manager / Managing Complex Trials
- Role
- Sr Clinical Trial Manager at ICON plc
- Location
- Plymouth, NC, US
- LinkedIn followers
- 500 followers
About Kim Cotten-West
With over 28 years of experience as a Sr. Study Manager and a Sr. Clinical Operations Lead, I have a proven track record of leading and overseeing the execution of global clinical trials, ensuring quality, compliance, and timeliness. I hold a CCRA® certification and two BS degrees in Textile Science and Marketing. As a Sr. Study Manager at Parexel, I specialize in clinical trials monitoring, proposals, project management, timelines, SOP, and Microsoft Office. I have successfully managed multiple complex and diverse projects, collaborating with cross-functional teams, clients, vendors, and stakeholders. I am passionate about advancing clinical trial research and delivering innovative solutions that improve lives.
Experience
Sr Clinical Trial Manager
Jul 2024 — Present · NC, US
Managed Phase I, II and three radioconjugate trials for metastatic castration-resistant prostate cancer across North America, Australia, and the UK. • Directed complex clinical operations, achieving enrollment targets while overseeing the CRO. • Collaborated with Clinical Manufacturing and Supply Chain teams to forecast drug supply requirements accurately. • Ensured effective vendor management and financial reconciliation, meeting study milestones and budget constraints.
Education
University of North Carolina at Greensboro
BS
Appalachian State University
Bachelor of Science - BS
Skills
- Clinical Research
- Clinical Trials
- Patient Recruitment
- Clinical Trial Management
- Strategic Planning
- Business Operations Management
- Marketing Strategy
- Ctms
- Project Management
- 21 Cfr Part 11
- Clinical Data Management
- Clinical Development
- Drug Development
- Clinical Monitoring
- Gcp
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