Clinical Research Coordinator Resume

This clinical research coordinator resume includes tips, content and appropriate words to draft an effective resume. This resume example is well-organized with clear headings, brief statements skills and responsibilities relevant to the position. You can use the tips to write an effective resume and get an interview call from your prospective employer.

A clinical research coordinator is a health-care professional who works under the supervision of a clinical trail associate or a physician investigator. Clinical research coordinator oversees and supervises the activities of staff involved in clinical trials.

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Sample Clinical Research Coordinator Resume

Paul Smith

2365 S Mayfield Ave
Chicago, IL 60652
Cell: 123-555-1234
email: paul@anymail.com

Summary of Objective:

Seeking a challenging and responsible position as a clinical research coordinator, where I can contribute my knowledge and experience in a health care organization.

Summary of Skills:

  • In-depth knowledge of the methods and principles of clinical practices
  • Extensive knowledge of human anatomy and physiology
  • Familiar with medical terminology and practices
  • Attention to detail with good research skills
  • Possess excellent project management, coordination and organizational skills
  • Excellent communication skills with ability to work in a team
  • Proficient in basic computer and software applications

Employment History:

Illinois General Hospital, Illinois

June 2005 till date

Clinical Research Coordinator

  • Maintain protocol requirements for patient visits, patient visit schedules, blood draw, test procedures, and drug accountability requirements
  • Complete all study documentation forms like case report forms and other specific research documents
  • Conduct patient care visits and assure that all the procedures are performed in compliance with the standard of the hospital
  • Interact with investigators to assure that the patient receives appropriate medical evaluation and care, when needed
  • Interact with clinical research associate to facilitate monitoring and database clean-up process
  • Attend meetings and conduct clinical research in compliance with all the applicable regulations

Institute of Health Sciences, Illinois

April 2003 to December 2004

Clinical Research Coordinator

  • Assign tasks of developing and preparing clinical research protocols
  • Responsible for organizing all aspects of medical research project of the organization
  • Coordinate the functions of different departments who work for clinical trial in investigating new health care terminologies, medicines, and procedures
  • Handle the responsibilities of managing investigation devices and maintaining database of the project
  • Perform clinical trial preparation like planning, assembling and instructing clinical trial team
  • Ensure that the medical professional that participates in the clinical research is qualified to fulfill the assigned duties
  • Handle responsibilities of conducting clinical trials of  clinical research staff

Educational Summary:

Achieved master’s degree in Public Health

University of Illinois in the year 2003

Achieved bachelor’s degree in Public Health

College of Medical Sciences, Illinois in the year 2000

Certification:

Certified Clinical Research Coordinator, Illinois

Personal Details:

Name: Paul Smith

Date of Birth: 13/01/1978

Employment Status: Full time

Relationship status: Single

Reference:

Will be pleased to furnish upon request

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