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Jessica Claire
  • , , 100 Montgomery St. 10th Floor
  • Home: (555) 432-1000
  • Cell:
  • resumesample@example.com
Professional Summary

Seasoned 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 23 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. Skilled at collecting specimens, dispensing medications and consulting with patients during the course of clinical research trials. Experienced in coordinating schedules, results and documentation. Knowledgeable and adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues. Enthusiastic and eager to contribute to team success through hard work, attention to detail and excellent organizational skills. Motivated to learn, grow and excel. Excellent reputation for resolving problems and improving patient satisfaction. Recognized consistently for performance excellence and contributions to success. Strengths are organization, multi tasking, communication with the doctors and companies and deadline driven.

Skills
  • Study protocols

  • Specimen collections

  • Good Clinical Practices

  • Medication dispensing

  • Trial management

  • Informed consent

  • Research SOPs understanding

  • Schedule Coordination

  • Multitasking abilities

  • Good listening skills

  • Excellent work ethic

  • Teambuilding

  • Self-motivated professional

  • Adaptability

Skills

Study protocols

:

Specimen collections

:

Good Clinical Practices

:

Medication dispensing

:

Trial management

:

Informed consent

:

Research SOPs understanding

:

Schedule Coordination

:

Multitasking abilities

:

Good listening skills

:

Excellent work ethic

:

Teambuilding

:

Self-motivated professional

:

Adaptability

:
Work History
Clinical Research Coordinator/Director, 09/2008 to Current
Arkansas UrologyBentonville, AR,
  • 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.
  • Gathered, processed and shipped lab specimens.
  • Followed informed consent processes and maintained records.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
  • 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.
  • Collected, evaluated and modeled collected data.
  • Conducted research, gathered information from multiple sources and presented results.
  • Completed all paperwork, recognizing any discrepancies and addressing them in a timely fashion.
  • Resolved problems, improved operations and provided exceptional service.
  • Developed and implemented performance improvement strategies and plans to promote continuous improvement.
Clinical Research Coordinator, 08/2005 to 08/2008
Arkansas UrologyBenton, AR,
  • Collected data and followed research protocols, operations manuals and case report form requirements.
  • Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
  • Collected, evaluated and modeled collected data.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Gathered, processed and shipped lab specimens.
  • Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
  • 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.
  • Followed informed consent processes and maintained records.
  • Developed team communications and information for meetings.
  • Resolved conflicts and negotiated mutually beneficial agreements between parties.
  • Used coordination and planning skills to achieve results according to schedule.
  • Developed and implemented performance improvement strategies and plans to promote continuous improvement.
  • Performed duties in accordance with all applicable standards, policies and regulatory guidelines to promote safe working environment.
Clinical Research Coordinator, 08/2004 to 05/2005
Arkansas UrologyPine Bluff, AR,
  • Collected data and followed research protocols, operations manuals and case report form requirements.
  • Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
  • Collected, evaluated and modeled collected data.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Gathered, processed and shipped lab specimens.
  • Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
  • 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.
  • Followed informed consent processes and maintained records.
  • Developed team communications and information for meetings.
  • Used coordination and planning skills to achieve results according to schedule.
  • Actively listened to customers' requests, confirming full understanding before addressing concerns.
  • Performed duties in accordance with all applicable standards, policies and regulatory guidelines to promote safe working environment.
Clinical Research Coordinator, 03/2002 to 05/2005
Retina Vitreous AssociatesCity, STATE,
  • Collected data and followed research protocols, operations manuals and case report form requirements.
  • Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
  • Collected, evaluated and modeled collected data.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Gathered, processed and shipped lab specimens.
  • Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
  • 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.
  • Followed informed consent processes and maintained records.
  • Developed team communications and information for meetings.
  • Used coordination and planning skills to achieve results according to schedule.
  • Performed duties in accordance with all applicable standards, policies and regulatory guidelines to promote safe working environment.
Education
High School Diploma: , Expected in 05/1990
Metro Baptis - Madison, TN,
GPA:
Certifications
  • Certified Phlebotomy
  • Training:
  • Human Research
  • Good Clinical Practice
  • Protecting Human Research Participants
Additional Information

I work with a company Targeted Medical Education and do the IRB submission for all the PI's across the US.

I also have a contract with a Breast Surgeon in CA and do his research home based.

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Resume Overview

School Attended

  • Metro Baptis

Job Titles Held:

  • Clinical Research Coordinator/Director
  • Clinical Research Coordinator
  • Clinical Research Coordinator
  • Clinical Research Coordinator

Degrees

  • High School Diploma

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