Summary
Overview
Work History
Education
Skills
Certification
Languages
Affiliations
Technical Skills
Timeline
Generic

Jessica Freeman

Mount Juliet,TN

Summary

As a dedicated professional, I bring a diverse skill set and a wealth of experience to any role I undertake. With a bachelor’s degree in nursing and extensive experience as a Clinical Research Coordinator, I have honed my ability to manage complex clinical trials, ensuring compliance with regulatory standards and providing top-notch patient care. My career journey also includes valuable insights gained as a Travel Advisor, where I mastered customer service and logistics management, enhancing my ability to plan and coordinate detailed travel itineraries efficiently.

Currently, I am expanding my expertise by pursuing a Master of Science in Data Analytics. This advanced education is equipping me with the analytical skills required to interpret large datasets, derive meaningful insights, and drive data-informed decision-making processes. I am excited to integrate my clinical research background with data analytics, aiming to contribute to innovative healthcare solutions and improved patient outcomes.

Overview

15
15
years of professional experience
1
1
Certification

Work History

Travel Advisor

Travelmation LLC
Mt. Juliet, TN
08.2024 - Current
  • Advised clients on travel destinations, transportation options, accommodations, and activities available at their destination.
  • Researched and compared different travel packages to ensure the best value for customers' money.
  • Assisted with booking flights, hotels, rental cars and other reservations.
  • Provided customers with detailed information about various tourist attractions and activities in different countries around the world.
  • Created itineraries tailored to each customer's individual needs and preferences.
  • Processed payments using a variety of methods including cash, credit cards or online payment services.
  • Developed marketing strategies to promote new products and services to potential customers via email campaigns or social media platforms.
  • Conducted follow-up calls with customers after their trip to ensure satisfaction and address any concerns they may have had during their travels.
  • Maintained up-to-date knowledge of local laws, customs and regulations in order to provide accurate advice to customers.
  • Attended conferences and training sessions related to the tourism industry in order to stay informed of current trends.

Home Trial Coordinator

FIRMA Clinical Research
Elk Grove Village, IL
08.2020 - 10.2023
  • Collaborate with sponsors, agencies, and sites to coordinate home trial visits.
  • Maintain study-related home trial visits in North America and regionally.
  • Create meeting agendas and minutes with sponsors, sites, and agencies, emphasizing quality and accuracy.
  • Prepare remote service providers and sites for patient visits.
  • Maintain specific study-related metrics.
  • Effective communication is essential to educate patients about trial procedures and expectations.
  • Scheduling and coordinating home visits for assessments and sample collection.
  • Familiarity with remote monitoring technologies and telemedicine platforms.
  • Knowledge of GCP (Good Clinical Practice) guidelines and FDA regulations.
  • Ensuring all trial activities comply with ethical and regulatory standards.
  • Preparation and maintenance of regulatory documents.
  • Collaborated with vendors to arrange contracts for services or products needed by the organization.

Clinical Research Coordinator

Tennessee Retina & Associates
Nashville, TN
04.2019 - 08.2020
  • Compiled trial-related documents into a master file, as required by the sponsor or regulatory agency.
  • Assisted in preparing periodic reports summarizing the progress of clinical studies.
  • Performed patient assessments, collected and analyzed data, and prepared reports.
  • Monitored patient safety during clinical trials according to established guidelines.
  • Coordinated investigator meetings, conference calls, and site initiation visits as needed.
  • Communicated effectively with investigators, study staff, sponsors, vendors, IRB personnel, and other stakeholders throughout the life cycle of the trial.
  • Facilitated resolution of protocol deviations or violations reported by sites or detected through monitoring activities.
  • Conducted quality assurance audits at research sites to ensure adherence to protocols, SOPs, regulations, and guidelines.
  • Reviewed CRFs for completeness and accuracy before database entry.
  • Conducted screening interviews to determine the eligibility of possible subjects.

Clinical Research Coordinator

St. Thomas West Research Institute
Nashville, TN
06.2017 - 04.2019
  • Coordinate and oversee clinical trials involving pacemaker wires and devices.
  • Identify and recruit eligible patients for pacemaker and device studies.
  • Conduct thorough screening processes to ensure patient eligibility and safety.
  • Provide detailed explanations of study procedures and potential risks to participants.
  • Schedule and conduct regular follow-up visits to monitor patient progress and device performance.
  • Collect, record, and manage accurate clinical data from patient visits and device readings.
  • Utilize electronic data capture (EDC) systems to ensure data integrity and compliance with study requirements.
  • Assist in the implantation and monitoring of pacemaker devices.
  • Work closely with cardiologists, surgeons, nurses, and other healthcare professionals to ensure smooth study operations.
  • Communicate effectively with study sponsors and stakeholders.
  • Monitor and report any adverse events or complications related to the devices.
  • Ensure timely and accurate documentation and communication of adverse events to regulatory authorities and study sponsors.

Oncology Patient Navigator

St. Thomas Midtown Hospital
Nashville, TN
10.2014 - 08.2017
  • Provide comprehensive education to patients and their families about lung cancer diagnosis, treatment options, and prognosis.
  • Offer emotional support and resources to help patients cope with their diagnosis and treatment journey.
  • Coordinate appointments and follow-up visits with oncologists, surgeons, and other healthcare providers.
  • Ensure timely scheduling of diagnostic tests, treatments, and procedures.
  • Facilitate communication between patients and healthcare teams to ensure cohesive care.
  • Assist patients in understanding and navigating the healthcare system.
  • Help patients access financial assistance programs, insurance coverage, and other resources.
  • Supply patients with educational materials, support group information, and access to community resources.
  • Assist in arranging transportation, lodging, and other logistical needs for patients traveling for treatment.
  • Advocate for patients' needs and preferences within the healthcare system.
  • Conduct follow-ups with patients to monitor their progress and address ongoing needs.
  • Track patient outcomes and report on the effectiveness of navigation services.
  • Work closely with a multidisciplinary team of healthcare professionals to provide comprehensive care.
  • Attend tumor board meetings and other collaborative discussions to advocate for patient needs.

Student Nurse Intern

Baptist Hospital
Nashville, TN
12.2009 - 10.2014
  • Provide basic patient care under the supervision of registered nurses.
  • Assist patients with daily activities, such as bathing, dressing, and eating.
  • Assist in administration of medications and treatments as directed by nurses and physicians.
  • Set up and maintain medical equipment and supplies in patient care areas.
  • Maintain accurate and detailed patient records.
  • Document patient observations and care activities.
  • Ensure all patient information is kept confidential and secure.
  • Communicate effectively with patients, families, and healthcare team members.
  • Report any changes in patient condition to supervising nurses or physicians.
  • Adhere to infection control protocols and safety procedures.
  • Ensure patient rooms and clinical areas are clean and sanitary.
  • Use personal protective equipment (PPE) as required.

Education

Bachelor of Science - Nursing

Cumberland University
Lebanon, TN
05-2010

Associate of Applied Science - Ophthalmology

Volunteer State Community College
Gallatin, TN
05-2003

Master of Science - Data Analytics

Southern New Hampshire University
Hooksett, NH

Skills

  • Excellent customer service
  • Creativity and innovation
  • Strong interpersonal skills
  • Cultural sensitivity
  • Exceptional communication
  • Administrative tasks
  • Study protocols
  • Documentation requirements
  • Research experience
  • Specimen handling
  • Specimen collections
  • Participant screening
  • Dispensing oversight
  • Phlebotomy
  • Adverse event tracking
  • Informed consent
  • Study monitoring
  • Patient recruitment
  • Research sops understanding
  • Good clinical practice
  • Participant recruitment
  • Analytical thinking
  • Leadership
  • Organized and detail-oriented

Certification

Tennessee Life Insurance Producer

NPN#20815409

Life, Accident, and Health

Languages

English
Professional

Affiliations

  • Traveling
  • Reading

Technical Skills

  • Microsoft Office Suite
  • SharePoint
  • EHR Systems
  • CTMS
  • Tello
  • eCRF
  • Study manager
  • eClinicalWorks

Timeline

Travel Advisor

Travelmation LLC
08.2024 - Current

Home Trial Coordinator

FIRMA Clinical Research
08.2020 - 10.2023

Clinical Research Coordinator

Tennessee Retina & Associates
04.2019 - 08.2020

Clinical Research Coordinator

St. Thomas West Research Institute
06.2017 - 04.2019

Oncology Patient Navigator

St. Thomas Midtown Hospital
10.2014 - 08.2017

Student Nurse Intern

Baptist Hospital
12.2009 - 10.2014

Bachelor of Science - Nursing

Cumberland University

Associate of Applied Science - Ophthalmology

Volunteer State Community College

Master of Science - Data Analytics

Southern New Hampshire University
Jessica Freeman