Krystal Canupp

Clinical Research Coordinator- LEAD/Manager

Timmonsville, SC 29161

ad3h8t@r.postjobfree.com

+1-912-***-****

• My goal is to obtain a professional position in a clinical research/medical work environment that promotes a team concept providing me the opportunity to apply my dynamic, resourceful, and skilled office abilities, detail-oriented attributes, and research training. I am seeking an environment where my professionalism can be used in a manner satisfying to your establishment's requirements, benefiting and supporting fellow employees and the study participants through job performance, accuracy, reliability, and the utmost courtesy.

Authorized to work in the US for any employer

Work Experience

Clinical Research Coordinator- LEAD

Strand GI Asociates and Endoscopy Center - Myrtle Beach, SC October 2021 to Present

• Start-up LEAD for all clinical studies at new research site/PI

• Equipment ordering, Calibration, and supply start-up for new research site and PI

• Temperature monitoring for the freezer, refrigerator, and ambient research equipment

• Recruiting possible study subjects for brand new research site

• Qualifying and consenting all participants

• Collect all data to send to the sponsor via self-reporting outcomes and surveys as well as all source documentation

• Collect blood samples and all medical tests required for the study

• Aliquote and centrifuge blood samples

• Venipuncture and subcutaneous injections when required per protocol

• Assist in colonoscopy procedures for certain biopsies needed per sponsor

• Package log, and ship blood samples daily

• Obtain vitals and medical history for study subjects

• Trained subjects on electronic devices for self-reporting outcomes and surveys

• follow all SOP and GCP required standards

• work independently under limited supervision of the PI (M.D.)

• conduct weekly/monthly meetings with the sponsor representative to evaluate all data collected for the study

• Report any and all SAE findings as well as Adverse Events

• Maintenance of all regulatory documents and monthly meetings with monitors assigned

• Complete all EDC entries and source documentation

• Follow study subjects well- being daily and retention of study subjects

• Conduct audits required by FDA

• Complete all start-up and closing documents needed for each study

• Complete all feasibility requests as well as walk-through evaluations from sponsors

• EKG testing and all required diagnostic testing per protocol

• Creating source documents when not provided by the sponsor

• Participated in all investigator meetings when requested

• Knowledge of CTA agreements and budgets between the site and sponsor

• Recruiting on behalf of the PI for any new and upcoming studies offered by potential sponsors.

• proficiency in CTMS systems for regulatory documents and source materials.

• IATA training Certificate

• GCP Certification

• work closely with an Artificial Intelligence company in surfacings new possible study participants

• extensive problem-solving experience and detailed oriented. Clinical Research Coordinator

Meridian Clinical Research - Savannah, GA

2016 to 2019

Screened and evaluated potential subjects for clinical trials

• Recruiting possible study subjects

• Qualifying and consenting all participants

• Collected all data to send to the sponsor via self-reporting outcomes and surveys as well as all source documentation

• Collected blood samples and all medical tests required for study

• Aliquoted and centrifuged blood samples

• Venipuncture and subcutaneous injections when required per protocol

• Packaged, logged and shipped blood samples daily

• Obtained vitals and medical history for study subjects

• Trained subjects on electronic devices for self reporting outcomes and surveys

• followed all SOP and GCP required standards

• worked independently under limited supervision of the PI (M.D.)

• conducted monthly meetings with the sponsor representative to evaluate all data collected for study

• Reported any and all SAE findings as well as Adverse Events

• Maintenance of all regulatory documents and monthly meetings with monitors assigned

• Completed all EDC entries and source documentation

• Followed study subjects well- being daily and retention of study subjects

• Conducted audits required by FDA

• Completed all start-up and closing documents needed for each study

• Completed all feasibility requests as well as walk through evaluations from sponsors

• EKG testing and all required diagnostic testing per protocol

• Creating source documents when not provided by sponsor

• Participated in all investigator meetings when requested

• Some knowledge in CTA agreements

• Recruiting on behalf of the PI for any new and upcoming studies offered by potential companies Medical Assistant

Low Country Dermatology - Savannah, GA

2013 to 2016

• Greeted and checked in all patients

• Collected co-pays and insurance information

• Prepare patient for exams and collected medical history

• Assisted with surgical procedures and treatments

• Cleaned medical instruments and patient rooms

• Collected vitals and blood samples

• Trained new staff on office procedures and patient care

• Obtained prior authorizations for patients and also refilled prescriptions Medical Assistant

Pee Dee Cardiology - Florence, SC

2012 to 2013

Triaged all patients prior to appointment

• Collected medical history and medication lists

• Performed EKG's prior to office visit

• Assisted with medical office procedures and exams

• Collected vitals and blood samples

• handled prescription refills

• cleaned and stocked all patient rooms daily

• ordered necessary supplies needed for patient rooms Medical Office Assistant

Winter Park Urology - Orlando, FL

2007 to 2009

• Thrived in an office setting that hosted fifteen urologists and three nurse practitioners, along with a surgical center and cancer center

• Checking patients in and out of the office for appointments and collecting coinsurance and copayment amounts

• Scheduling appointments for surgery and other minor procedures

• Collecting urinalysis and sending them to the back office or to outside labs

• Entered new patient records

• Extensive training in complete paperless office/patient records

• Aided in the process of refilling prescriptions and answering phone calls for the provider on call Education

Associate of Science Degree in Medical Assisting

Keiser University - Orlando, FL

February 2010 to June 2012

High School Diploma

West Florence High School - Florence, SC

2006

Skills

• Clinical Research

• Clinical Trial

• CRC

• Microsoft Office

• Business Management

• Training & Development

• Patient Education

• Medical Office Experience

• Data Collection

• GCP

• Experience Administering Injections

• Laboratory Experience

• Recruiting

• Medical Records

• EMR Systems

• Vital Signs

• Phlebotomy

• Medical Scheduling

• Venipuncture

• Anatomy Knowledge

• Clinical Trials Management Systems (2 years)

• Management

• EMR systems

• Medical records

• Data collection

• Training & development

• Laboratory experience

• Clinical research

• Vital signs

• Anatomy knowledge

• AI

Additional Information

References can be given upon request

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