Summary
Overview
Work History
Education
Skills
Timeline
Generic

Samantha Korn

Monroe

Summary

Qualified Clinical Research Site Manager with a solid background as a Certified Clinical Research Coordinator. Extensive experience at IMA Clinical Research, excelling in clinical trial management, team leadership, and regulatory submission and upkeep. Proven reliability and adaptability with extensive experience in employee training facilitation to build, support and lead a successful team. Skilled in ICH guidelines ensuring compliance and quality in research practices.

Overview

17
17
years of professional experience

Work History

Certified Clinical Research Coordinator

IMA Clinical Research
05.2015 - Current
  • Coordinated clinical trial activities to ensure compliance with regulatory standards and protocols.
  • Managed patient recruitment efforts, enhancing participant retention and engagement throughout studies.
  • Developed and maintained relationships with key stakeholders, including investigators and sponsors, to facilitate study progress.
  • Oversaw data collection processes, ensuring accuracy and integrity of research findings across multiple trials.
  • Trained and mentored junior staff on best practices in clinical research methodologies and compliance requirements.
  • Conducted regular audits of study documentation to uphold quality assurance standards and address discrepancies promptly.
  • Maintained high ethical standards in research practices, adhering to Good Clinical Practice guidelines and safeguarding patient rights.
  • Increased protocol compliance by providing comprehensive training and support to study team members.
  • Enhanced patient enrollment by implementing efficient recruitment strategies and streamlining the screening process.
  • Ensured site readiness for audits and inspections by maintaining a well-organized, detailed, and accurate study documentation system.
  • Reduced study deviations by closely monitoring patient progress and promptly addressing any issues or concerns.
  • Gathered, processed, and shipped lab specimens.
  • Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
  • Prepared and maintained regulatory documents for clinical trial submissions.
  • Streamlined regulatory submissions by efficiently preparing documentation, including informed consent forms, serious adverse event reports, and institutional review board materials.
  • Supported positive relationships between patients and research teams through empathetic communication and compassionate care coordination efforts during clinical trials participation.

Receptionist

Gastroenterology Clinic
04.2008 - 04.2010
  • Managed front desk operations, ensuring efficient visitor check-in and appointment scheduling.
  • Oversaw daily office activities, promoting a welcoming atmosphere that enhanced client relations.
  • Confirmed appointments, communicated with clients, and updated client records.
  • Supported office efficiency by performing clerical tasks such as data entry, photocopying, scanning, and faxing documents.
  • Handled sensitive information with discretion while maintaining strict confidentiality standards.
  • Handled incoming and outgoing package deliveries, working with vendors to complete special requests and track missing packages.
  • Maintained accurate records and documentation of incoming calls and messages for timely follow-up.
  • Coordinated office supplies inventory, facilitating seamless procurement processes to support daily operations.

Education

Clinical Research Coordinator Certification - Clinical Research

The Association of Clinical Research Professionals
05-2024

No Degree - Surgical Technology

Career Technical College
Monroe, LA
01-2007

Certification - Phlebotomy

University of Louisiana At Monroe
Monroe, LA
01-2005

High School Diploma -

Crowville High School
Crowville, LA
05-2004

Skills

  • ICH guidelines
  • Clinical trial management
  • IRB submissions
  • Monitoring visit preparation
  • Sponsor communication
  • Site initiation visits
  • Study closeout procedures
  • Site management
  • Team building
  • Training facilitaion and onboarding

Timeline

Certified Clinical Research Coordinator

IMA Clinical Research
05.2015 - Current

Receptionist

Gastroenterology Clinic
04.2008 - 04.2010

Clinical Research Coordinator Certification - Clinical Research

The Association of Clinical Research Professionals

No Degree - Surgical Technology

Career Technical College

Certification - Phlebotomy

University of Louisiana At Monroe

High School Diploma -

Crowville High School