You want to bring your unique skill sets to an upcoming clinical trial. In order to compete for the position, you need a stellar resume. That can be easier said then done, especially in this fierce job market. Put the spotlight on your noteworthy skills like formulating trial parameters and metrics as well as processing and managing trial dates right in your resume summary. Make sure to highlight your organizational skills in addition to specific experience in trials you’ve worked with. If organizing a complex clinical trial sounds easier then writing a resume, you aren’t alone. Creating a winning resume is tough. So, before you sit down at the computer to compose yours, take a peak at our clinical trial associate resume examples for a bit of inspiration.

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clinical trial associate resume example

 

Clinical Trial Associate Resume Questions

1. What format should your clinical trial associate resume be in?

Your resume format should match the job (or more specifically, its required skills and attributes). For example, if you were applying for a job in the arts and entertainment industry, then recruiters might expect a creative resume employing multiple images and unique resume fonts. For a clinical trial associate, you should go with a clean and straightforward professional format. Companies hiring for a such a position care more about your skill set than they do your creativity. If you do not know exactly what such a format should look like, consult the clinical trial associate resume sample.

2. How many bullet points do you include with each job in a clinical trial associate resume?

The answer to this question depends on the amount of information you have to share. You could probably dedicate an entire page of your resume template to each of your previous positions, yet remember that employers only want to know relevant details. A good rule of thumb to follow is to not include any previous responsibilities or achievements that do not apply to the job you are seeking. You will notice that in the clinical trial associate resume sample, the applicant dedicates three bullets to each job. This is the minimum number that you should include. Conversely, you should not list more than five.

3. What should you write in the experience section of your clinical trial associate resume?

Now that you know how many bullet points to use, the question becomes what information you should include therein. Again, only share details of job duties that will be similar to what you would do in this new job. Remember to also include information about the professional achievements you have earned, being careful to include detailed metrics about each one. When formatting the information in your experience section, remember to begin each bullet point with an action word (e.g., “directed” or “guided” as opposed to “was responsible for”). This makes it easier for readers to envision you performing those tasks.

4. How do you share soft skills on a clinical trial associate resume?

A job as a clinical trial associate requires an extensive knowledge of technical programs and industry-specific regulations. Thus, you should list your familiarity with those in your resume. At the same time, you should also demonstrate your communication skills, as well as your ability to work well under pressure. Note how in the clinical trial associate resume sample, the applicant lists “detail-oriented” and “organized” in the highlights section. These are soft skills that are not necessarily unique to researchers or healthcare workers yet still have application in those jobs. Therefore, you need to reserve a place for them in your resume.

5. How long should a clinical trial associate resume be?

Your resume needs to be long enough to adequately introduce yourself to recruiters yet short enough to keep their attention. By following the right format and organizing information into dedicated sections and bullet points, you can easily fit all of the information needed on a single page. If you need guidance on how to structure your resume to keep to one page, our resume builder tool offers step-by-step instructions on how to do just that.

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Resume Text

 

Seth Johnson 123 Fake Street City, State, Zip Code Cell: 000-000-0000 email@email.com

Summary

Dedicated Clinical Trial Associate who can provide comprehensive support for clinical research and projects. Experienced with formulating trial parameters and metrics, organizing and maintaining trial tracking systems, and processing and managing trial data. Specialize at conducting patient screenings and deducing eligibility.

Highlights

 

  • Trial protocols
  • Patient eligibility
  • Data processing and management
  • Regulation and compliance
  • Supply and inventory
  • Scheduling
  • Detail oriented
  • Organized

    Work Experience

    February 2009 to December 2014 Company Name — City, State Clinical Trial Associate -Managed and monitored the supply inventory of tools and equipment for trials -Produced, processed and managed trial documentation, produced trial reports detailing progression, deadlines, goals, and updates -Organized the scheduling of clinical trials, assisted in the screening of patients and the development of protocols May 2004 to January 2009 Company Name — City, State Clinical Trial Associate -Prepared documentation for clinical trials including protocol details, case reports and patient consent -Organized and monitored the progression of tracking systems to determine trial progression -Monitored clinical trials for compliance with state and federal regulations April 2000 to March 2004 Company Name — City, State Clinical Trial Associate -Assisted in the screening and interviewing of potential trial applicants, assessed eligibility -Developed and implemented clinical trial protocols, monitored progression of trial to ensure maintenance to protocols -Managed and processed incoming trial data, formulated graphs and statistical reports

    Education

    1999 Texas Tech University, City, State Bachelor of Science in Biomedical Studies

 

Related Skills

  • Medication dispensing
  • Specimen collections
  • Study protocols
  • Research SOPs understanding
  • Informed consent
  • Good Clinical Practices
  • Trial management
  • Maintenance and Repair
  • MS Office
  • Organization and Time Management