Clinical Research Analyst Resume Example & Writing Guide

Use this Clinical Research Analyst resume example and guide to improve your career and write a powerful resume that will separate you from the competition.

Clinical research analysts are medical professionals who help researchers collect data for new drug or device trials. They’re also responsible for designing studies, analyzing data, and reporting results back to their teams.

Clinical research analysts work closely with clinical trial coordinators and other members of the research team to create study protocols and identify potential participants based on their demographics, medical history, and other factors. They also help develop questionnaires and other tools researchers use to measure outcomes and collect data.

If you have a passion for research and science, and enjoy working on complex projects that require critical thinking and attention to detail, clinical research may be the perfect career for you. Here are some tips and an example resume to help you write a fantastic clinical research analyst resume that hiring managers will love.

Michael Garcia
Chicago, IL | (123) 456-7891 | [email protected]

Highly analytical and detail-oriented clinical research associate with over five years of experience in the pharmaceutical industry. Proven ability to manage clinical trials from start to finish, assess and summarize data, and develop presentations for senior management. Seeking a position that will allow me to use my skills and experience to make a positive impact on patient outcomes.

Rush University Jun '10
M.S. in Clinical Research Administration
University of Illinois at Chicago Jun '06
B.S. in Biological Sciences
Company A, Clinical Research Analyst Jan '17 – Current
  • Managed the clinical research projects from initiation to completion, including study design and implementation of protocols for new studies.
  • Developed a comprehensive understanding of the disease area under investigation as well as knowledge about current treatment options available in the marketplace.
  • Assisted with preparation of regulatory submissions (INDs, NDAs) by providing input on study designs and data analyses and assisted with preparing responses to FDA requests for additional information during review process.
  • Provided support for all aspects of clinical trial conduct including vendor management, site selection/management, monitoring activities at sites, etc., ensuring compliance with regulations and company policies & procedures.
  • Participated in development of budgets for each project based on timelines established by the Project Manager and provided oversight over expenditures related to specific projects through regular reporting to PMO leadership regarding budget status and expenditure trends across active projects.
Company B, Clinical Research Analyst Jan '12 – Dec '16
  • Assisted in the development of a new clinical trial for patients with chronic pain, resulting in an increase in patient satisfaction by 15%
  • Conducted weekly data analysis and reported findings to research team, contributing to increased patient participation rates by 20%
  • Managed all aspects of clinical trials as directed by senior management, including budgeting and scheduling
  • Supervised daily operations at medical center laboratory, ensuring quality control standards were met
  • Maintained accurate records on all patients involved in clinical trials, tracking their progress over time
Company C, Research Assistant Jan '09 – Dec '11
  • Researched and compiled data on the effects of climate change in a specific region using satellite imagery, field notes, and statistical analysis;
  • Wrote reports summarizing research results and presented findings at academic conferences;
  • Assisted with lab maintenance tasks such as cleaning equipment and repairing instruments, reducing project downtime by 50%.
  • Certified Clinical Research Professional
  • Certified Clinical Research Coordinator
  • Clinical Research Associate

Industry Knowledge: Clinical Trials, Biostatistics, Study Design, Statistical Analysis, Clinical Research, IRB, HIPAA
Technical Skills: SAS, SPSS, Microsoft Office Suite, Google Analytics, Google Docs, Salesforce, Constant Contact, Typeform
Soft Skills: Communication, Teamwork, Problem-Solving, Research, Critical Thinking, Time Management

How to Write a Clinical Research Analyst Resume

Here’s how to write a clinical research analyst resume of your own.

Write Compelling Bullet Points

When you’re writing bullet points, it can be tempting to simply list your responsibilities. But that’s not enough to make a strong impression. Instead, you should use your bullet points to demonstrate your value by highlighting your accomplishments, results, and contributions.

For example, rather than saying you “conducted clinical trials,” you could say you “conducted clinical trials for new drug treatment, resulting in a 20% decrease in patient symptoms.”

The second bullet point paints a much clearer picture of what you did and the results of your work. And that’s what hiring managers want to see—so make sure to include that kind of detail in your bullet points!

Identify and Include Relevant Keywords

When you apply for a clinical research analyst job, your resume will likely be scanned by an applicant tracking system (ATS) for certain keywords. If your resume doesn’t include enough of the right keywords, your application might not make it past the initial screening process.

The best way to make sure you have the right keywords on your resume is to take a look at some of the job postings you’re applying for and try to match them up with the skills and experience you have. Here are some common clinical research analyst keywords to get you started:

  • Good Clinical Practice (GCP)
  • Clinical Trials
  • Clinical Research
  • Electronic Data Capture (EDC)
  • Protocol
  • CRO Management
  • Clinical Development
  • Standard Operating Procedure (SOP)
  • Clinical Monitoring
  • Protocol Development
  • Oncology
  • Good Clinical Practice (GCP) Training
  • Clinical Data Management
  • Regulatory Submissions
  • SAS
  • CRO Services
  • Clinical Operations
  • Clinical Data Capture
  • Biotechnology
  • Statistics
  • Clinical Research Management
  • Medicine
  • Project Management
  • Microsoft Access
  • Analytical Skills
  • Medical Writing
  • Management
  • Clinical Trials Management System (CTMS)
  • Clinical Development Operations
  • MedDRA

Showcase Your Technical Skills

As a clinical research analyst, you will be responsible for analyzing data and developing reports. Therefore, it is essential that you list your technical skills prominently on your resume. Some of the skills that you should highlight include your proficiency in statistical analysis, data mining, and modeling. You should also list any experience you have with specific software programs, such as SAS, SPSS, and Stata. Including this information on your resume will show recruiters that you have the skills and experience necessary to be successful in the role.


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