Summary
Overview
Work History
Education
Skills
Timeline
Generic

Damien Patterson

Covington,GA

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 Three years of related experience to a challenging new role.

  • 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.
  • Knowledgeable Clinical Research Coordinator Lead adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues.
  • Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.
  • Detail-oriented team player with strong organizational skills. Ability to handle multiple projects simultaneously with a high degree of accuracy.

Overview

17
17
years of professional experience

Work History

Clinical Research Coordinator Lead

Care Access Research
Boston, MA
04.2022 - Current
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
  • Collected data and followed research protocols, operations manuals, and case report form requirements.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Followed informed consent processes and maintained records.
  • Gathered, processed, and shipped lab specimens.
  • Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
  • Collected, evaluated, and modeled collected data.
  • Skilled at working independently and collaboratively in a team environment.
  • Developed and maintained courteous and effective working relationships.
  • Used strong analytical and problem-solving skills to develop effective solutions for challenging situations.
  • Exercised leadership capabilities by successfully motivating and inspiring others. Helped to manage the day to day operations for my given sites
  • Worked flexible hours across night, weekend and holiday shifts.
  • Demonstrated strong organizational and time management skills while managing multiple projects.
  • Identified issues, analyzed information and provided solutions to problems.
  • Proven ability to learn quickly and adapt to new situations.
  • Cultivated interpersonal skills by building positive relationships with others.
  • Adherrance to ICH GCP, ALCOA, state and federal guidelines and regulations

Clinical Research Coordinator

Digestive Healthcare
Atlanta, GA
10.2019 - Current
  • Plan and coordinate projects that advanced medical treatment, through broad aim of clinical research trials
  • Executed multiple duties in clinical drug trials, to include vital signs, IV placement and infusions, subcutaneous injecions, phlebotomy and specimen collections, screening and patient assessments, perform liver Fibroscans, EKG and Holter Monitoring, urine pregnancy and drug screens, administering clinical trial medications and healthcare to study participants as instructed by Principal Investigator in accordance with clinical research protocols
  • Exhibited Analytical, Communication, Time Management, Organizational Skills and Attention to Details in various trials, to include;
  • Intercept (NASH-Non Alcoholic -Steatohepatitis)
  • Genfit (PBC)
  • AMAX (Crohns’s Disease)
  • AMAP (Ulcerative Colitis)
  • Guardant (Colorectal)
  • ALMANAC (Colorectal)
  • PFIZER (NASH-Non Alcoholic -Steatohepatitis)
  • CYMABAY (PBC)
  • Novo-Nordisk (Peripheral Aerial Disease- (PAD) & Type II Diabetes)
  • ARENA- 206 (EOE)
  • APD 334 (Ulcerative Colitis)
  • Collect, recorded and maintained data on source documents with timely completion of Case Report Forms
  • Promoted good clinical practices in conduct of clinical investigations
  • Compliance with trial protocols and regulatory requirements
  • Responded to and answering of queries of medical monitors and study sponsors
  • Facilitated in developing source documents for new clinical research projects
  • Conducted telephone and face to face interviews with potential research patients, also sending emails for follow up visits or correspondence per protocol study
  • Active recruitment of potential study subjects and assisted lead study coordinator with close-out visits
  • Attended site initiation visits & site monitor visits in addition to other meetings for various studies
  • Completed all site training requirements including GCP, IATA, OSHA training, site SOP review and training, and department training
  • Ensured that all study supplies and kits have been received and documented
  • Training in several study portals to include: IMEDI-DATA, CRIO, SMARTSTART, STUDYTEAM, ICON, & ELI-LILLY
  • Respond appropriately and timely with documentation of all AE’s and SAE’s in accordance with protocol guidelines for all studies
  • IP accountability and compliance with all study protocols as needed
  • Maintained all subjects' binders of documentation and Daily monitoring of IP storage temperatures.

Phlebotomy Team Lead

Labcorp/Crawford Long- Emory Hospital
Atlanta, GA
08.2012 - 06.2018
  • Collection of patient samples and other fluids for testing and research purposes
  • Properly identified patients with updates in CLIA Systems using ID or other documentation of means
  • Ensure optimal quality in preservation of patient health and quality of samples
  • Skills with presence of mind, people skills and attention to details
  • Upkeep of medical records on specimen and fluid testing
  • Adhere to all relevant health and safety standards in clinical setting.

Licensed Clinical Laboratory Assistant/ Assistant Phlebotomy Supervisor

Madison Parish Hospital
Tallulah, LA
06.2006 - 08.2011
  • Responsible for Supervisor and Overseeing of Phlebotomists including training, quality assurance measures and completion of required CEU credits
  • Venipuncture of patients as required including adults, elderly, children and infants
  • Corresponds regularly with hospitals, physicians, personnel, external clients, and outside labs regarding patient information and reports
  • Works as a MLT benchwork testing on Serology, Chemistry, Hematology, Special Urine specimens
  • Including manual differentials, urinalysis and microscopic analysis
  • Active participation in quality assurance and quality control programs specifically Biorad Unity control programs
  • Thorough understanding of quality control graphs, Wesgard Rules, L-J Plots, Histograms and Imprecision Bias and Markers
  • Participation in CAP surveys, CLIA and JCAHO Inspections as well as Emergency Preparedness
  • Performs patient and method correlations on analyzers.

Education

IV Infusion With Certification -

Georgia School of Phlebotomy
Sandy Springs, GA
05.2022

Two Year Certification -

Atlanta Metropolitan College of Atlanta
Atlanta, GA
05.2020

Clinical Laboratory Sciences -

Louisiana State Board of Medical
Tullulah, LA
06.2007

Certified Phlebotomy by American Society of Phlebotomy Technicians (ASPT) - Phlebotomy

University of Louisiana
Tullos, LA
05.1997

Skills

  • Study protocols
  • Research SOPs understanding
  • Trial management
  • Good Clinical Practices
  • Informed consent
  • Schedule Coordination
  • Organization and Time Management
  • Attention to Detail
  • Excellent Communication
  • Siemens Dimension System Advanced Diagnostics and Troubleshooting
  • Siemens Dimension Clinical Chemistry System Advanced Education
  • Siemens QCC Power Pak
  • GCP and IATA Training and Certification
  • OSHA & EPIC Information Systems
  • Study Protocols and Informed Consent
  • American Heart Association CPR Certified
  • Schedule Coordination
  • Adverse Event Documentation
  • Phlebotomy
  • Medical Histories and Vital Statistics
  • Participant Recruitment
  • Specimen Collection
  • Patient Safety
  • Lab Specimens and Collections
  • Investigator Meetings
  • Regulatory Knowledge
  • Research Sops Understanding

Timeline

Clinical Research Coordinator Lead

Care Access Research
04.2022 - Current

Clinical Research Coordinator

Digestive Healthcare
10.2019 - Current

Phlebotomy Team Lead

Labcorp/Crawford Long- Emory Hospital
08.2012 - 06.2018

Licensed Clinical Laboratory Assistant/ Assistant Phlebotomy Supervisor

Madison Parish Hospital
06.2006 - 08.2011

IV Infusion With Certification -

Georgia School of Phlebotomy

Two Year Certification -

Atlanta Metropolitan College of Atlanta

Clinical Laboratory Sciences -

Louisiana State Board of Medical

Certified Phlebotomy by American Society of Phlebotomy Technicians (ASPT) - Phlebotomy

University of Louisiana
Damien Patterson