Pharmacovigilance Associate Resume Example & Writing Guide
Use this Pharmacovigilance Associate resume example and guide to improve your career and write a powerful resume that will separate you from the competition.
As a pharmacovigilance associate, you’ll play an important role in the safety of the drugs that millions of people use every day. You’ll be tasked with monitoring the effects of medications, identifying potential side effects, and helping to resolve issues that arise.
Because the safety of patients is so important, this field is highly regulated. You’ll need a solid understanding of federal regulations like FDA guidelines and Good Pharmacovigilance Practices (GVP). You’ll also need to be familiar with industry best practices, like those outlined by the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH).
Here are some tips and an example to help you write a fantastic pharmacovigilance resume that hiring managers will love.
How to Write a Pharmacovigilance Associate Resume
Here’s how to write a resume of your own.
Write Compelling Bullet Points
Bullet points are the most important part of your resume because they’re the only thing hiring managers will have to go on when they’re trying to decide whether or not to interview you. So it’s crucial that you use them to your advantage by highlighting your most impressive accomplishments.
For example, rather than saying you “assisted with data collection for clinical trials,” you could say you “assisted with data collection for clinical trials for leading pharmaceutical company, resulting in 100% data collection rate on all projects.”
The second bullet point is much stronger because it provides specific details about what you did and the outcome of your work. It also includes a quantifiable result (100% data collection rate).
Identify and Include Relevant Keywords
When you apply for a pharmacovigilance associate role, your resume is likely to be scanned by an applicant tracking system (ATS) for certain keywords. ATS programs rank resumes based on the number of relevant keywords that are found throughout the document. If your resume doesn’t have enough relevant keywords, the ATS might not forward it to a recruiter.
To make sure your resume makes it past the ATS, focus on including keywords that are commonly found in pharmacovigilance associate job postings. Here are a few examples:
- Pharmacovigilance
- Drug Safety
- Clinical Trial Management System (CTMS)
- Vigilance
- Pharmacoepidemiology
- Electronic Medical Record (EMR)
- Oncology
- Oncology Pharmacy
- U.S. Food and Drug Administration (FDA)
- MedDRA
- Drug Development
- Adverse Event Reporting
- Drug Information
- Electronic Data Capture (EDC)
- Standard Operating Procedure (SOP)
- Hazard Analysis and Critical Control Points (HACCP)
- Good Clinical Practice (GCP)
- Clinical Research
- Phase I – III Clinical Trials
- Pharmacology
- Good Laboratory Practice (GLP)
- Clinical Pharmacology
- R&D
- Molecular Biology
- Biosafety
- Life Sciences
- Molecular Cloning
- Cell Culture
- Validation
- Microbiology
Showcase Your Technical Skills
Pharmacovigilance associates need to be proficient in a number of software programs and databases in order to effectively do their jobs. These might include the FDA’s Adverse Event Reporting System (FAERS), the European Medicines Agency’s (EMA) European Database of Suspected Adverse Drug Reactions (EudraVigilance), and the World Health Organization’s (WHO) Uppsala Monitoring Centre (UMC) database. In addition, pharmacovigilance associates need to be able to use statistical software programs, like SAS and R, to analyze data.