Kathleen Wilson

Kathleen Wilson Email and Phone Number

Experienced remote Clinical Research Coordinator with a background in experimental psychology dedicated to advancing healthcare through innovative clinical trials. @
Kathleen Wilson's Location
Charlottesville, Virginia, United States, United States
About Kathleen Wilson

Clinical Research Coordinator with 7 years of experience in academic and pharmaceutical research. Skilled in managing multiple research sites, coordinating remote decentralized trials and collaborating with diverse teams. Demonstrated expertise in patient recruitment and retention, database management and navigating complex research regulations and policies. Recognized for strong organizational and communication abilities with a passion for optimizing trial processes and driving successful study outcomes. Strong communication and organizational skills, ensuring seamless collaboration among research teams, sponsors and regulatory bodies. Seeking to leverage expertise to take on increased responsibilities and drive successful trial outcomes.

Kathleen Wilson's Current Company Details
VAUMC

Vaumc

Experienced remote Clinical Research Coordinator with a background in experimental psychology dedicated to advancing healthcare through innovative clinical trials.
Kathleen Wilson Work Experience Details
  • Vaumc
    Executive Administrative Manager
    Vaumc Oct 2024 - Present
    Remote
    Executive administrator to the Mountain View District of the VAUMC.
  • Care Access
    Clinical Research Coordinator
    Care Access Jan 2023 - Jul 2024
    Remote
    Managed the screening process for over 150 study patients, achieving a 90% retention rate through efficient informed consent and follow-up procedures.Led assessment scheduling, logistics coordination, and technology support for patients, central raters, and study investigators, improving communication efficiency by 30%.Ensured data accuracy through timely EDC entry, maintaining a 98% data integrity rate across various technological systems.Acted as a subject matter expert for co-coordinators, research assistants and external sites and provided training and resolving study-related issues.Analyzed protocols to ensure study endpoints were achieved in compliance with GCP, FDA and HIPAA regulations.
  • Javara
    Clinical Research Coordinator
    Javara May 2022 - Oct 2022
    Forest, Virginia
    Managed clinical trial activities, adhering to SOPs, GCP guidelines and study protocols for multiple studies.Conducted and documented informed consent processes for over 100 participants, ensuring regulatory compliance and high participant satisfaction.Coordinated participant visits, study-related procedures and communications, leading to a 20% improvement in participant compliance.Identified and performed outreach to prospective patients, contributing to a 60% increase in recruitment rates.Prepared for and participated in monitoring visits, audits and inspections. maintaining audit-ready study documentation.
  • Wcg
    Clinical Research Coordinator
    Wcg Oct 2021 - May 2022
    Lynchburg, Virginia, United States
    Prescreened participants using EMR (AthenaOne), achieving recruitment goals for an ophthalmology study within 6 months.Developed and implemented community outreach strategies that enhanced patient recruitment by 50%.Built rapport with participants, leading to an 85% retention rate through effective communication and support.Conducted EDC data entry and maintained documentation in compliance with regulatory requirements.
  • University Of Virginia
    Clinical Research Coordinator
    University Of Virginia Jul 2020 - Jan 2021
    Charlottesville, Virginia, United States
    Managed multiple clinical trials in a medical setting, ensuring adherence to GCP and institutional protocols.Recruited, consented and conducted follow-up with over 150 participants, maintaining high levels of protocol adherence.Facilitated audit preparations and responded to data clarification requests within regulatory timelines.Prepared and submitted IRB documents, annual reports and study amendments to the Human Investigation Committee.
  • University Of Utah
    Clinical Research Coordinator
    University Of Utah Aug 2018 - Jun 2020
    Salt Lake City, Utah, United States
    Coordinated research studies focusing on chronic pain management, substance use and mindfulness interventions.Managed eTMF and eCTMS, updating study documentation as required by FDA, DOD and VA guidelines.Conducted clinical assessments, including the Mini International Neuropsychiatric Interview and other measures to evaluate opioid use patterns.Recruited participants through clinical settings, media and healthcare provider referrals, surpassing enrollment targets by 30%.
  • University Of Massachusetts Dartmouth
    Study Coordinator
    University Of Massachusetts Dartmouth Aug 2015 - May 2017
    North Dartmouth, Massachusetts, United States
    Managed databases, participant recruitment, scheduling and correspondence, ensuring data accuracy and confidentiality throughout study procedures.Prepared documentation for proposals, IRB reviews and grants and supervised undergraduate training in laboratory protocols.Developed experimental designs and administered psychological tests, ensuring precise scoring and adherence to research protocols.Conducted literature reviews and wrote experiment summaries for publication, contributing to the dissemination of research findings.

Kathleen Wilson Education Details

Frequently Asked Questions about Kathleen Wilson

What company does Kathleen Wilson work for?

Kathleen Wilson works for Vaumc

What is Kathleen Wilson's role at the current company?

Kathleen Wilson's current role is Experienced remote Clinical Research Coordinator with a background in experimental psychology dedicated to advancing healthcare through innovative clinical trials..

What schools did Kathleen Wilson attend?

Kathleen Wilson attended University Of Massachusetts Dartmouth, Randolph College.

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