Whether you want to work as a clinical research assistant or in any other type of field, a professional CV is the best way to stand out from other applicants and highlight your best skills, experience, and personality traits. Writing a high-quality CV requires excellent writing skills and an understanding of how your CV should be formatted. To help you get started, we have compiled a list of guidelines for writing yours. Use it along with the PDF CRA CV example to help you write a CV that draws in hiring managers.

 

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Abby Smith

123 Fake Street, City, State, Zip Code

E: email@email.com P: 000-000-0000

Professional Summary

Professional and thorough clinical research assistant with more than 10 years of experience in a wide variety of research situations. Proven communicator with excellent written and verbal speaking and comprehension skills. Thorough, detail-oriented, and able to manage time wisely. Strives to be friendly and upbeat to facilitate a comfortable working environment for all involved.

Skills
  • Active listening skills that include giving the person speaking full attention, understanding the points made, asking questions for clarification when necessary, and providing feedback.
  • Excellent critical thinking, judgment, and decision-making abilities to identify strengths and weaknesses in a study and define ways to make the study better for both researchers and patients.
  • Fluently speak, read, and write English and Spanish with an excellent command of spelling and grammar in both languages.
  • Ability to be engaging, friendly, patient, and understanding when teaching patients about new studies and helping them determine if they qualify.
  • Ability to manage time appropriately and ensure that detailed reports are turned in on time.
Experience
Clinical Research Assistant
January 2011 – Present

 

 
 




 
  • Maintains research records, including regulatory forms, records of drug dispensation, and case reports.
  • Monitors studies to ensure patients and researchers are complying with institutional, local, state, and federal protocols.
  • Assesses patients to determine eligibility for specific studies based on interviews, medical history, and discussion with researchers.




Clinical Research Administrator
December 2009 – January 2011

 

 
 




 
  • Established and maintained relationships between clients and researchers to ensure a productive and cooperative research environment.
  • Recorded information and interpreted its meaning to create reports for researchers to use when determining how to proceed with the study.
  • Developed teams of patients to participate in specific research studies, and communicated expectations and benefits with them to prepare them for the study.




Clinical Research Associate
October 2003 – December 2009

 

 
 

 

 
  • Oversaw patients by recording reactions to drug trials, including allergies, illnesses, and how patients felt both physically and emotionally.
  • Maintained patient records and study information using a wide range of computer hardware and software to enter and process data.
  • Trained new clinical research associates on office procedures, patient interaction, and computer programs related to research studies.

 

Education
Internship
2002

 

 
Arizona State University
 
Bachelor of Medical Studies
2002

 

 
Arizona State University
 
Hobbies and Interests

In my spare time, I enjoy reading medical journals and other research publications to learn about advances in the medical field. I also like to volunteer to read to pediatric and geriatric patients at the local hospital. Hiking, baking low-carb treats, and swimming take up most of the rest of my time.

 

 

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Clinical Research Assistant Job Overview and Tips

What Does a CRA Do?

A clinical research assistant is responsible for assisting researchers in planning, directing, and otherwise coordinating clinical research projects. They assist researchers in finding patients who have the appropriate physical and mental health history to participate in particular studies and then assist in ensuring all researchers and patients are in compliance with protocols, including those of the institution as well as local, state, and federal governing authorities. In many cases, CRAs are responsible for evaluating and analyzing data and providing preliminary results to researchers. The attached CRA CV example PDF goes into more detail regarding expected job duties and qualifications. Use it in conjunction with the following guidelines when creating your own CV.

Tips for Creating a Great CRA CV

Implement these guidelines on your CV using our CV maker to ensure it is professional and gains the attention of hiring managers.

  • Do use proper formatting. Include paragraphs for the professional summary and hobbies and interests, but use bullet points for most other information. This makes it easy for hiring managers to skim for the most important information.
  • Do not include information that is too personal, such as your sexual orientation, political views, or religious views. Avoid anything controversial.
  • Do use strong action words that show the type of work you did. Avoid using phrases such as responsible for.
  • Do not include irrelevant information, such as your GPA, high school information, or clubs you belonged to that do not benefit your current career path.
  • Do proofread your work thoroughly and multiple times to ensure all information is correct and that there are no spelling or grammatical errors.

Related Skills

  • Medical device trials
  • Medication testing
  • Database maintenance
  • Patient recruitment
  • Specimen collection
  • Pharmaceutical sponsor compliance
  • Ethics committee guidelines
  • Specimen collections
  • Study protocols
  • Good Clinical Practices

We can help you build your professional CV

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