Summary
Overview
Work History
Education
Skills
Timeline
Generic
Janel Lollis

Janel Lollis

Clinical Research Coordinator
Summerville,SC

Summary

Dedicated Clinical Research Coordinator experienced in complying with study protocols, standard operating procedures and good clinical practices. Practiced problem-solver with strong attention to detail. Prepared to offer twenty years of experience in the field and take on a fast-paced position.

Overview

20
20

Years of Healthcare experience

Work History

Clinical Research Coordinator

CareAccess MSO
09.2021 - Current
  • Kept patient care protocols and clinical trial operations in compliance.
  • Assessed records of each patient, reviewed databases and checked referrals to locate potential research study participants.
  • Adhered to standards in areas involving data collection, research protocols and regulatory reporting.
  • Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
  • Participated in educational training, activities and professional development programs.
  • Adhered to good clinical practices, operating procedures and regulatory requirements.
  • Evaluated proof of eligibility and consent for participants.
  • Reviewed site regulatory binder to check collection procedures and completeness of paperwork.
  • Attended investigator meetings to provide framework for successful research studies by establishing responsibilities.
  • Attended meetings and reported on activities and resolutions.
  • Recruited and selected potential research subjects.

Clinical Research Coordinator

Three Wire
Summerville, SC
10.2020 - 10.2021
  • Kept patient care protocols and clinical trial operations in compliance.
  • Assessed records of each patient, reviewed databases and checked referrals to locate potential research study participants.
  • Adhered to standards in areas involving data collection, research protocols and regulatory reporting.
  • Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
  • Took vital signs and collected medical histories as part of study protocols.
  • Conducted screening interviews to determine eligibility of possible subjects.
  • Educated participants on studies and anticipated outcomes.
  • Placed orders for medications to be used in studies.
  • Promoted high customer satisfaction by resolving problems with knowledgeable and friendly service.
  • Understood and followed oral and written directions.
  • Worked successfully with diverse group of coworkers to accomplish goals and address issues related to our products and services.
  • Planned and completed group projects, working smoothly with others.

Phlebotomist

LabCorp
Summerville, SC
06.2010 - 09.2020
  • Located veins suitable for puncture to draw blood using sterilized needles, vials and other equipment.
  • Identified patients using proper procedures prior to specimen collection.
  • Prepared and packaged specimens for courier transport.
  • Maintained fully-stocked phlebotomy cart, carrier and station.
  • Delivered quality patient care by completing accurate and timely collection and transport of clinical specimens according to established procedures.
  • Obtained blood samples for medical testing and transfusion through venipuncture or capillary puncture.
  • Centrifuged blood specimens in test tubes and capillary tubes to separate cells and sediment from blood serum.
  • Promoted blood specimen integrity for laboratory testing using accurate selection of collection tubes and correct technique.
  • Transported specimens following established protocol for temperature and light.
  • Observed patient for unusual reactions or events to take appropriate action under established guidelines.
  • Collected specimens for drug screens, paternity tests and alcohol tests.
  • Verified collection orders and communicated discrepancies to nurses.
  • Conducted various blood tests and updated results into paper and electronic charts.
  • Processed client payments and collected appropriate billing information.

Education

Bachelor of Science - Health Sciences

Trident University International
Cypress, CA
05.2020

Skills

  • Trial Oversight
  • Research Experience
  • Documentation Requirements
  • Patient Safety
  • Reviewing Data Standards
  • Interactive Management
  • Data Evaluation
  • Research and Development
  • Status Reporting
  • Site Management
  • Clinical Research Monitoring Experience
  • Monitoring Visits
  • Quality Control
  • Patient Recruitment Strategies
  • Clinical Documentation
  • Organizational Skills

Timeline

Clinical Research Coordinator

CareAccess MSO
09.2021 - Current

Clinical Research Coordinator

Three Wire
10.2020 - 10.2021

Phlebotomist

LabCorp
06.2010 - 09.2020

Bachelor of Science - Health Sciences

Trident University International
Janel LollisClinical Research Coordinator