Summary
Overview
Work History
Education
Skills
Websites
References
Timeline
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Christy Williams

Covington

Summary

Detail-oriented Clinical Research Coordinator and proud U.S. Navy veteran with a solid foundation in healthcare operations, regulatory compliance, and patient-centered care. Proven ability to manage clinical trials from initiation to close-out, ensuring protocol adherence, accurate documentation, and ethical standards. Skilled in collaborating with multidisciplinary teams, maintaining data integrity, and navigating complex regulatory environments. Eager to contribute expertise in organization, communication, and problem-solving to advance clinical research and improve patient outcomes.

Overview

19
19
years of professional experience

Work History

Clinical Research Coordinator

Biopharma Informatic
Mandeville
02.2023 - Current
  • Conduct informed consent discussions, ensuring participant understanding and proper documentation.
  • Monitor participant safety and report adverse events in accordance with study protocols.
  • Dispense investigational products and provide dosage instructions per protocol.
  • Collect, process, and ship biological specimens following safety and protocol guidelines.
  • Complete and verify case report forms (CRFs), resolving data queries with accuracy.
  • Report protocol deviations to PI and regulatory bodies as required.
  • Coordinate site activities and ensure compliance with study protocols.
  • Oversee data entry and management in electronic data capture systems.
  • Facilitate communication between study teams, participants, and external stakeholders.
  • Ensure adherence to regulatory requirements and ethical standards.
  • Assist in the development and implementation of study protocols and SOPs.
  • Lead coordination for multi-center trials, ensuring alignment with sponsor expectations.
  • Manage site-level timelines, visit scheduling, and resource allocation.
  • Support audit readiness and assist with sponsor monitoring visits.

Medical Assistant

Dimitri Dermatology/Sanova Dermatology
Metairie
11.2014 - 02.2023
  • Accurately documented and organized physician notes in Electronic Medical Records (EMR), ensuring up-to-date and compliant patient records.
  • Collected and recorded patient medical history, vital signs, and presenting concerns with precision and professionalism.
  • Managed administrative responsibilities including scheduling, filing, and maintaining organized medical records.
  • Educated patients on treatment plans and post-care instructions, enhancing patient understanding and satisfaction.
  • Maintained a clean and well-stocked clinical environment, ensuring readiness for patient care and procedures.
  • Demonstrated strong multitasking and prioritization skills in a fast-paced outpatient setting.
  • Collaborated effectively with physicians, nurses, and administrative staff to support seamless clinic operations.
  • Applied attention to detail and ethical decision-making in handling sensitive patient information and interactions.

Logistics Specialist

U.S. Navy Active Duty
Norfolk
04.2006 - 09.2013
  • Managed and processed material receipts for medical storerooms.
  • Maintained fiscal oversight of travel and procurement budgets
  • Maintained detailed records for inventory, shipping, and controlled materials.
  • Coordinated customer service requirements and logistics operations.
  • Supervised storeroom operations and conducted inventory audits.
  • Tracked financial obligations and reconciled travel accounts.
  • Resolved vendor disputes and led logistics teams to meet operational goals.
  • Ensure accurate recordkeeping, accountability, and vendor coordination for supply chain effectiveness.

Education

Some College (No Degree) - General Studies

Chattahoochee Valley Community College
Phenix City, AL

Some College (No Degree) - Pre-Nursing

Delgado Community College
New Orleans, LA

Skills

  • Clinical Trial Coordination
  • Informed Consent Process
  • Adverse Event Reporting
  • Regulatory Compliance (IRB, FDA)
  • Specimen Collection & Phlebotomy
  • Electronic Data Capture (EDC) Systems
  • Case Report Form (CRF) Management
  • Participant Recruitment & Retention
  • SOP & Protocol Adherence
  • Effective communication
  • Problem solving
  • Attention to detail
  • Medication dispensing
  • Good clinical practices

References

References available upon request.

Timeline

Clinical Research Coordinator

Biopharma Informatic
02.2023 - Current

Medical Assistant

Dimitri Dermatology/Sanova Dermatology
11.2014 - 02.2023

Logistics Specialist

U.S. Navy Active Duty
04.2006 - 09.2013

Some College (No Degree) - General Studies

Chattahoochee Valley Community College

Some College (No Degree) - Pre-Nursing

Delgado Community College
Christy Williams