Catherine Jay Email & Phone Number | I am a knowledgeable SOCRA Certified Clinical Research Professional with 10+ years of experience and expertise coordinating, monitoring, and auditing Phase 1-3 clinical trials. My capacity to collect and manage data, ensure quality, and improve processes pair well with my ability to communicate effectively with stakeholders of diverse ranks during face-to-face, group, and presentation settings along with my instinct for organizing and motivating others to achieve goals on time and with excellence. Along with my experience, my database knowledge is significant as I am proficient in REDCap, iMedNet, Medidata Rave, InForm, Oracle, and Microsoft Access. My core skills include but are not limited to: GCP/FDA/ICH Regulations, Clinical Research SOPs Stakeholder Communication, Data Collection & Management, Quality Assurance, Process Improvement, Report Writing & Editing, Team Collaboration, Speaking & Presentations, Technical Acumen, Critical Thinking, and Problem Solving.

Catherine Jay

I am a knowledgeable SOCRA Certified Clinical Research Professional with 10+ years of experience and...
Denver, Denver, United States

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Catherine Jay’s Location Denver, Denver, United States

Catherine Jay’s Current Industry Caris Life Sciences

Catherine Jay’s Prior Industry Surgone | University Of Colorado Anschutz Medical Campus | Ppd

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Clinical Research Associate II

2022-06-01T00:00:00.000Z - Present

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2018-05-01T00:00:00.000Z - 2020-06-01T00:00:00.000Z

Clinical Research Auditor

2016-12-01T00:00:00.000Z - 2018-05-01T00:00:00.000Z

Senior Research Study Coordinator

2007-01-01T00:00:00.000Z - 2010-06-01T00:00:00.000Z

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Catherine Jay is a I am a knowledgeable SOCRA Certified Clinical Research Professional with 10+ years of experience and expertise coordinating, monitoring, and auditing Phase 1-3 clinical trials. My capacity to collect and manage data, ensure quality, and improve processes pair well with my ability to communicate effectively with stakeholders of diverse ranks during face-to-face, group, and presentation settings along with my instinct for organizing and motivating others to achieve goals on time and with excellence. Along with my experience, my database knowledge is significant as I am proficient in REDCap, iMedNet, Medidata Rave, InForm, Oracle, and Microsoft Access. My core skills include but are not limited to: GCP/FDA/ICH Regulations, Clinical Research SOPs Stakeholder Communication, Data Collection & Management, Quality Assurance, Process Improvement, Report Writing & Editing, Team Collaboration, Speaking & Presentations, Technical Acumen, Critical Thinking, and Problem Solving.