Clinical Research Coordinator Resume

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Career Objective:

Highly-qualified, organized, and certified ‘Clinical Research Coordinator’ with over 6+ years of experience in gathering information, performing drug trials and following protocols. Adept in ensuring CRF, maintaining medicine supplies and shipping specimens for tests to laboratories to provide quality care for patients. Team player with excellent management and interpersonal skills.

Summary of Qualifications:

  • Sound knowledge of clinical research laws and procedures, including patient consent, performing screening to test eligibility, and ensuring accurate documentation

  • Familiar with monitoring patient’s response to the administered medicines for the clinical trial, identifying side effects, and sending test specimens to the laboratory

  • Skilled in maintaining records of clinical trials such as case report forms, availability of the drugs, and dispensed reports

  • Adept in researching and contacting participants willing and matching for the clinical trials

  • Proficiency in operating computer applications such as MS Office for maintaining clinical trial data sheets, and responding to mail/calls as required

  • Ability to work in a team using exceptional prioritization, organizational, and communication skills

Work Experience:

Clinical Research Coordinator

OhoHealth, Chicago, IL

June 2016 – Present

  • Monitoring patient’s progress to evaluate effectiveness of the therapy applied during clinical trial, and assisting to schedule regular appointments with the concerned doctor

  • Ensuring essential documentation and recording of patient’s research data in appropriate files as per institutional, and regulatory requirement

  • Serving as a primary point of contact for the research participants, pharmaceutical sponsors, and regulatory hospitals to coordinate collection of study reports as well as advertise the trials to recruit participants

  • Estimating funds necessary for the clinical trial, and finding sponsors for funding

  • Performing various clinical research duties such as coordinating services, scheduling procedures, creating and maintaining case packages, and monitoring charges

  • Handling and assisting with the administrative activities associated with the clinical trials by reviewing medical records or conducting screenings for recruitment of study patients with the help of interviews and QOL questionnaires

Assistant Clinical Research Coordinator

Barbara Ann Karnamos Cancer Institute, Chicago, IL

October 2014 – May 2016

  • Monitored clinical trials by overseeing various factors, including patient enrollment, assessing they meet the specified criteria and reviewing Case Report Forms (CRF)
  • Performed assessments of the hospital’s pharmacy department to ensure that the clinical trial supplies are stored and dispensed appropriately
  • Helped to design study flow sheets, data forms, and source documents by gathering, and interpreting medical, surgical and laboratory data related to clinical trial subjects

  • Coordinated with the team to perform and record duties related to protocol specific treatments, and assured collection as well as shipment of samples to the concerned hospitals

  • Ensured all the study-related requirements are documented in accordance to the protocol guidelines

Clinical Research Associate

Mayo Clinic, Chicago, IL

March 2012 – September 2014

  • Worked with the team responsible for running clinical trials for testing new drug

  • Reviewed and ensured the ISF files are updated and collected essential documents as well as information from patients involved in drug trials

  • Performed various duties related to trials, including consenting patients, abstracting data from medical records, completing case report forms, and entering data into database

  • Assisted in conducting interviews of the individuals interested in clinical trials to record premorbid history information, and performed physical assessments before granting permission

  • Participated in seminars conducted by ethics committee of the pharmacist companies to safeguard rights, safety, and well-being of the trial subjects


Nursing Intern

Mayo Clinic, Chicago, IL

July 2010 – February 2012

  • Worked in the out-patient department to perform physical assessment
  • Monitored heart rate, blood pressure and health complaints for preparing patient’s paper
  • Drafted reports on patients’ response for certain drug, and their unusual behavior

  • Provided health-care services to patients in various wards including pediatric, neonatal and trauma center

  • Prepared list of medicines and other equipment in shortage to place timely orders

  • Attended weekly training sessions to learn ways to assess, diagnose, and evaluate patients’ need by communicating with physicians and nurse supervisor


  • Bachelor’s Degree in Nursing

    University of Illinois, Chicago, IL



  • Certified Clinical Research Coordinator

    University of Illinois, Chicago, IL



  • The Association for Clinical Research Professionals – Member since 2014


On request.

Related Links :

Clinical Research Coordinator Cover Letter

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