Summary
Overview
Work History
Education
Skills
Accomplishments
Certification
FDA- GCP Regulations
Timeline
Generic

Anashia Reese

Orlando,FL

Summary

Focused Clinical Research Coordinator well-versed in study protocols, standard operating procedures and general trial oversight. Excellent problem-solving abilities with a detail-oriented nature. Ready to bring Number years of related experience to a challenging new role.

Knowledgeable Job Title adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues.

Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Certified in Area.

Skilled at collecting specimens, dispensing medications and consulting with patients during the course of clinical research trials. Experienced in coordinating schedules, results and documentation.

Multi-talented Job Title consistently rewarded for success in planning and operational improvements. Experience in policy development and staff management procedures positively impacting overall morale and productivity.

Job Title with over Number years of successful experience in Skill and Skill. Recognized consistently for performance excellence and contributions to success in Industry industry. Strengths in Skill and Skill backed by training in Area of study.

Experienced Job Title with over Number years of experience in Industry. Excellent reputation for resolving problems, improving customer satisfaction, and driving overall operational improvements. Consistently saved costs while increasing profits.

Overview

2
2
years of professional experience
1
1
Certification

Work History

Lead Clinical Research Coordinator

Precision Research & Solutions
Altamonte Springs, FL
05.2020 - 06.2020
  • Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
  • Collected data and followed research protocols, operations manuals and case report form requirements.
  • Followed informed consent processes and maintained records.
  • Collected, evaluated and modeled collected data.
  • Monitored unit budget to meet financial objectives for spend rate and funding.
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Gathered, processed and shipped lab specimens.
  • Devoted special emphasis to punctuality and worked to maintain outstanding attendance record, consistently arriving to work ready to start immediately.
  • Developed team communications and information for Type meetings.
  • Resolved Type problems, improved operations and provided exceptional client support.
  • Transported Product or Service to customer locations Timeframe.
  • Resolved conflicts and negotiated mutually beneficial agreements between parties.
  • Monitored social media and online sources for industry trends.
  • Maintained excellent attendance record, consistently arriving to work on time.

Clinical Research Assistant

Florida Premier Research Institute
Winter Park, FL
09.2018 - 10.2019
  • Managed updates and input for patient information database.
  • Assisted with research protocol development.
  • Educated patients regarding all facets of clinical study participation.
  • Demonstrated advanced knowledge of federal regulatory compliance guidelines.
  • Coordinated clinical trials focused on disorders such as Name and Name.
  • Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Collected data and followed research protocols, operations manuals and case report form requirements.
  • Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
  • Collected, evaluated and modeled collected data.
  • Gathered, processed and shipped lab specimens.
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Followed informed consent processes and maintained records.
  • Maintained excellent attendance record, consistently arriving to work on time.
  • Devoted special emphasis to punctuality and worked to maintain outstanding attendance record, consistently arriving to work ready to start immediately.
  • Handled Number calls per Timeframe to address customer inquiries and concerns.
  • Developed team communications and information for Type meetings.

Education

Medical Assistant

Florida Career College
Orlando, FL
10.2017

Skills

  • Research SOPs understanding
  • Medication dispensing
  • Informed consent
  • Study protocols
  • MS Office
  • Supervision
  • Business operations
  • Project organization
  • Database organization Specimen handling
  • Phlebotomy
  • CPR certification
  • Laboratory operations
  • Good Clinical Practices
  • Specimen collections
  • Trial management
  • Process improvement
  • Relationship development
  • Operational improvement
  • Problem resolution
  • Data evaluation
  • Ethics protocol adherence Documentation requirements Laboratory results management Research experience
  • Strong background in FDA drug safety guidelines Strong clinical background
  • HIPAA trained
  • Updated and maintained information accuracy within patient data

Accomplishments

  • Used Microsoft Excel to develop inventory tracking spreadsheets.
  • Resolved product issue through consumer testing.
  • Documented and resolved Issue which led to Results.

Certification

  • First Aid/CPR Certified
  • ServSafe

FDA- GCP Regulations

Compliance Ensurance as per FDA-GCP Regulations

Site-Management

Initiations Experience

Closeouts

Site Monitoring

Timeline

Lead Clinical Research Coordinator

Precision Research & Solutions
05.2020 - 06.2020

Clinical Research Assistant

Florida Premier Research Institute
09.2018 - 10.2019

Medical Assistant

Florida Career College
Anashia Reese