LiveCareer-Resume

research coordinator resume example with 20+ years of experience

Jessica
Claire
resumesample@example.com
(555) 432-1000,
Montgomery Street, San Francisco, CA 94105
:
Summary

Dedicated Clinical Research Coordinator with over 20 years of experience in complying with study protocols, standard operating procedures and good clinical practices. Practiced problem-solver with strong attention to detail. Knowledge of FDA and GCP principles and regulations. Committed to providing support to the project team and executing responsibilities as instructed.

Skills
  • Feasibility assessments experience
  • Data organization
  • Project oversight
  • Equipment maintenance
  • Phlebotomy
  • Laboratory results management
  • Dispensing oversight
  • Documentation requirements
  • Trial oversight
  • Case report management
  • Research experience
  • Specimen handling
  • Scheduling proficiency
  • Critical thinking
  • Problem resolution
  • Leadership
  • Work ethic
  • Microsoft Office
Education and Training
Colorado Christian University Denver, CO Expected in 12/2020 Associate Degree in Healthcare Administration : Healthcare - GPA :
ACRP , Expected in 06/2008 Certified Clinical Research Coordinator : - GPA :
George Washington University, The Washington, DC Expected in Bachelor of Science : Clinical Research Administrator - GPA :
Experience
Balyasny Asset Management - Research Coordinator
New York, NY, 10/2018 - Current
  • Recognized issues and developed immediate resolutions to address and alleviate concerns.
  • Adhered to standards in areas involving data collection, research protocols and regulatory reporting.
  • Obtained informed consent of research subjects or guardians
  • Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
  • Conducted informed consent presentations and maintained documentation.
  • Assessed records of each patient, reviewed databases and checked referrals to locate potential research study participants.
  • Kept patient care protocols and clinical trial operations in compliance.
  • Organized, analyzed and modeled study data.
  • Collected, processed and delivered specimens from trial participants.
  • Detailed results and conclusions in professionally-prepared documents, reports and presentations.
  • Checked electronic data capturing systems for integrity and compliance.
  • Maintained laboratory record system to document key information on specimen collection, identification, quality control and other factors.
  • Sanitized workstations and salon equipment to reduce risk of infection.
  • Reviewed packages and medication bottles for proper labeling before distributing to patients.
  • Checked medications for content, accuracy and completeness of drug packaging and labeling.
  • Maintained compliance with state and federal drug laws.
Balyasny Asset Management - Research Coordinator/ Office Manager
Austin, TX, 04/2011 - 09/2018
  • Research Allergy, Asthma and Sinus Assoc.
  • Oversaw receiving and organizing correspondence, answering and forwarding calls and creating business letters and records.
  • Keyed in customer contacts and delivery dates to update details in company databases.
  • Managed office inventory and placed new supply orders.
  • Handled scheduling and managed timely and effective allocation of resources and calendars.
  • Trained and mentored administrative staff members in company policies, daily task execution and industry best practices.
  • Coordinated office activities and operations to secure efficiency and compliance with company policies.
  • Reduced financial discrepancies by accurately managing accounting documentation.
  • Mentored and provided ongoing support to research team, providing training in research design and conduct.
  • Kept patient care protocols and clinical trial operations in compliance.
  • Adhered to standards in areas involving data collection, research protocols and regulatory reporting.
  • Obtained informed consent of research subjects or guardians
  • Performed preliminary physical tests to accurately record results in patient history summary.
  • Educated patients about medications, procedures and physician's instructions.
  • Maintained inventory, vaccination and product expiration logs to record updated documentation for tracking purposes.
  • Efficiently performed insurance verification and pre-certification and pre-authorization functions.
Balyasny Asset Management - Research Coordinator
Boston, MA, 02/2007 - 04/2011
  • Juggled multiple projects and tasks to ensure high quality and timely delivery.
  • Prioritized and organized tasks to efficiently accomplish service goals.
  • Worked closely with team members to deliver project requirements, develop solutions and meet deadlines.
  • Worked successfully with diverse group of coworkers to accomplish goals and address issues related to our products and services.
  • Managed clinical research trials involving women's health, neurological and gynecological disorders.
Mid Atlantic Retina - Research Coordinator
Mays Landing, NJ, 12/2004 - 02/2007
  • Cleaned and sterilized lab area, tools and equipment.
  • Followed strict aseptic techniques to protect patients when collecting blood and tissue samples.
  • Drew blood from patients to collect samples using venipuncture and following aseptic techniques.
  • Documented and updated patient data on electronic medical charts, maintaining accuracy and confidentiality.
  • Observed and recorded vital signs and reported changes to physicians or nurses.
  • Adhered to all safety and infection control precautions and regulations.
  • Supported healthcare teams in consistently delivering timely and quality care according to company standards.
  • Obtained informed consent of research subjects or guardians
  • Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
  • Assessed records of each patient, reviewed databases and checked referrals to locate potential research study participants.
  • Kept patient care protocols and clinical trial operations in compliance.
Medical Research Unlimited - Research Assistant
City, STATE, 07/2001 - 12/2004
  • Reviewed new research literature to remain current with examination procedures.
  • Conducted qualitative and quantitative analysis on data assigned.
  • Used Microsoft Word and PowerPoint to prepare reports, presentations and research results.
  • Completed research assignments by organizing data, generating spreadsheets and drafting reports.
  • Generated reports and made recommendations based on research outcomes.
  • Prepared documentation of research procedures and data gathered for dissemination to staff members.
  • Researched data processing operations and conducted proof of concept monitoring after new process implementation.
  • Monitored experiments and maintained detailed records of experiments and outcomes.
  • Organized and maintained records, inventory and materials.
  • Assisted in research for development of new products and processes.
  • Adhered to standards in areas involving data collection, research protocols and regulatory reporting.
  • Managed informed consent forms, personal waivers and other critical paperwork.
  • Designed survey instruments and questionnaires to obtain desired research data.
Languages
Spanish :
Professional
Negotiated :
English :
Professional
Negotiated :

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Resume Overview

School Attended

  • Colorado Christian University
  • ACRP
  • George Washington University, The

Job Titles Held:

  • Research Coordinator
  • Research Coordinator/ Office Manager
  • Research Coordinator
  • Research Coordinator
  • Research Assistant

Degrees

  • Associate Degree in Healthcare Administration
  • Certified Clinical Research Coordinator
  • Bachelor of Science

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