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Jessica Claire
  • , , 609 Johnson Ave., 49204, Tulsa, OK 100 Montgomery St. 10th Floor
  • Home: (555) 432-1000
  • Cell:
  • resumesample@example.com
Professional Summary

Detail-oriented Clinical Research Associate well-versed in coordinating operations, managing sites and drafting detailed clinical reports. Knowledgeable about action planning, database locking and standard operating procedures. Supports participant recruitment and management to meet research objectives. 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.

Skills
  • Trial methodologies
  • Subject tracking tools
  • Data Collection, Review, and Evaluation
  • Report writing
  • Coordinating site operations
  • Protocol adherence
  • Project monitoring
  • EMR: Epic and Cerner proficient
  • Team Player
  • Excellent Interpersonal Skills
  • Excellent communication
  • Time Management
  • Patient Safety
  • Leadership
  • Training & Development
  • Collaboration
  • Multitasking abilities
  • Research Monitoring
  • Study Protocols
  • Trial study center set up
  • · Accountability
  • EDC
Work History
Sr Clinical Research Associate 111, 02/2019 to Current
EndologixSanta Rosa, CA,
  • Followed drug storage procedures to comply with protocols and SOP requirements.
  • Traveled to investigative sites to conduct site qualification, initiation, interim monitoring and close-out visits to maintain and enforce regulatory compliance.
  • Adhered to procedures, practices and regulatory requirements to maintain health, safety and environmental compliance.
  • Reviewed participant eligibility and consent documentation to help researchers achieve accurate and meaningful results.
  • Set up and disbanded trial study centers to manage clinical study activities for [Number] sites.
  • Promoted awareness of project-specific quality and performance standards to support documentation, communication and understanding.
  • Gathered and organized clinical trial documentation to meet rigorous standards for site approval.
  • Submitted routine [Type] reports and follow-up letters to facilitate internal and external communication.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Liaised with clinical investigator to identify, assess and resolve site performance, quality and compliance issues.
Clinical Research Associate, 11/2015 to 07/2018
Planet PharmaBristol, PA,
  • 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.
  • Followed informed consent processes and maintained records.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Developed and maintained courteous and effective working relationships.
  • Participated in continuous improvement by generating suggestions, engaging in problem-solving activities to support teamwork.
  • Worked closely with [job title] to maintain optimum levels of communication to effectively and efficiently complete projects.
  • Maintained excellent attendance record, consistently arriving to work on time.
Clinical Trial Assistant, 03/2012 to 03/2015
XYZCity, STATE,
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Collected data and followed research protocols, operations manuals and case report form requirements.
  • Followed informed consent processes and maintained records.
  • Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
  • 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.
  • Collected, evaluated and modeled collected data.
  • Worked to maintain outstanding attendance record, consistently arriving to work ready to start immediately.
  • Completed all paperwork, recognizing any discrepancies and addressing them in a timely fashion.
  • Prepared a variety of different written communications, reports and documents to ensure smooth operations.
Education
Bachelor of Science: Biochemistry, Expected in
Lagos State University - Overseas,
GPA:
Associate of Science: Business Administration, Expected in 07/2015
Georgia State University-Perimeter College - Clarkston, GA,
GPA:

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Resume Overview

School Attended

  • Lagos State University
  • Georgia State University-Perimeter College

Job Titles Held:

  • Sr Clinical Research Associate 111
  • Clinical Research Associate
  • Clinical Trial Assistant

Degrees

  • Bachelor of Science
  • Associate of Science

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