Drug Safety Associate Resume Example & Writing Guide

Use this Drug Safety Associate resume example and guide to improve your career and write a powerful resume that will separate you from the competition.

Drug safety associates are part of the team that ensures prescription drugs are safe for patients to use. They conduct research and develop reports on the adverse effects of certain medications, and they also play a role in product labeling and marketing efforts.

Because drug safety is such a highly regulated field, drug safety associates must follow strict guidelines when conducting their research. They must also follow set guidelines when writing their reports. Because of the sensitive nature of their work, drug safety associates must be extremely careful not to disseminate information that might be misleading or inaccurate.

Here’s some tips and an example to help you write a great drug safety associate resume that hiring managers will love.

Jennifer Thomas
New York City, NY | (123) 456-7891 | [email protected]

Proven drug safety associate with experience in conducting literature reviews and developing safety narratives for regulatory submissions. Possesses extensive knowledge of drug development process and strong critical thinking skills. Seeking an opportunity to utilize expertise in a challenging and innovative pharmaceutical company.

University at Buffalo Jun '10
B.S. in Biology
Company A, Drug Safety Associate Jan '17 – Current
  • Assisted in the development of a new drug safety database and assisted with data entry for clinical trials, observational studies, and post-marketing surveillance activities.
  • Provided support to study teams by entering patient enrollment information into the database as well as performing other clerical tasks such as copying documents, scanning documents, etc.
  • Performed statistical analyses on various databases including adverse event reporting systems (AERS), medical records review system (MRRS), electronic health record (EHR) and laboratory information system (LIS).
  • Reviewed AERS reports for potential signals related to product quality or safety issues and reviewed MRRS case report forms for medication errors that may have contributed to an adverse event or injury.
  • Analyzed LIS data to identify trends in healthcare utilization patterns among patients enrolled in clinical trials or observational studies which can be used to improve care delivery processes within the organization.
Company B, Drug Safety Associate Jan '12 – Dec '16
  • Assisted in the development of a new drug safety program that reduced adverse events by 25%
  • Conducted weekly inspections on all equipment and supplies to ensure quality control standards were met
  • Maintained an inventory of over 100 different drugs, including hazardous chemicals and radioactive isotopes
  • Supervised 10+ employees within the department’s budget constraints while maintaining a high level of customer service
  • Collaborated with other departments to improve processes for greater efficiency and cost-effectiveness
Company C, Clinical Research Assistant Jan '09 – Dec '11
  • Screened potential participants for eligibility according to study criteria and enrolled eligible participants.
  • Obtained informed consent from participants and ensured that all required documentation was completed prior to participant enrollment.
  • Conducted study visits with participants according to protocol and collected data using various methods such as interviews, surveys, or blood draws.
  • Certified Clinical Research Professional
  • Certified Quality Auditor
  • Certified Regulatory Affairs Professional

Industry Knowledge: Pharmaceutical, FDA, QA/QC, Pharmacokinetics, Pharmacodynamics
Technical Skills: Microsoft Office Suite, Access, SAS, SPSS
Soft Skills: Communication, Teamwork, Leadership, Problem Solving, Time Management, Organization

How to Write a Drug Safety Associate Resume

Here’s how to write a drug safety associate resume of your own.

Write Compelling Bullet Points

Bullet points are the most important part of your resume because they’re the first thing recruiters will read. And since they’re so important, it’s crucial that you use them to your advantage by crafting compelling bullet points that highlight your experience and skills.

The best way to do this is to focus on the results of your work. So rather than saying you “conducted research,” you could say you “conducted research to identify new drug candidates for rare diseases, resulting in the discovery of two new drug candidates.”

The second bullet point is much more interesting and compelling because it provides more detail about what exactly you did and the outcome of your work.

Identify and Include Relevant Keywords

When you apply for a drug safety associate role, your resume will likely be scanned by an applicant tracking system (ATS) for certain keywords. These programs look for specific terms related to the job, like “safety testing” or “pharmaceuticals” in order to determine whether you’re a good fit for the position. If you don’t have enough of the right keywords on your resume, the ATS might discard your application.

To make sure this doesn’t happen, use this list of common drug safety associate keywords as a starting point:

  • Drug Safety
  • Good Clinical Practice (GCP)
  • Clinical Trials
  • Electronic Data Capture (EDC)
  • Standard Operating Procedure (SOP)
  • CRO Management
  • Biotechnology
  • Oncology
  • Pharmacovigilance
  • Laboratory Skills
  • Life Sciences
  • Pharmacology
  • Validation
  • Good Manufacturing Practice (GMP)
  • Drug Development
  • Life Sciences Research
  • Molecular Biology
  • Regulatory Affairs
  • In Vitro Techniques
  • Clinical Development
  • SDS
  • Drug Discovery
  • Life Sciences
  • Cell Culture
  • Good Laboratory Practice (GLP)
  • U.S. Food and Drug Administration (FDA)
  • Biochemistry
  • Analytical Chemistry
  • Microsoft Access
  • Clinical Trials Management System (CTMS)

Showcase Your Technical Skills

As a drug safety associate, you will need to be proficient in the use of various software programs to effectively do your job. These programs may include electronic health records (EHR) systems, patient monitoring systems, and clinical data management systems. Additionally, you should be familiar with statistical software programs like SAS and R. Being able to list your level of expertise in each of these areas will show that you are a valuable asset to any pharmaceutical company.


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