Pharmacovigilance Scientist Resume Example & Writing Guide

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

Pharmacovigilance is the safety monitoring of prescription drugs once they hit the market. And pharmacovigilance scientists are responsible for identifying and monitoring side effects, performing research studies, and analyzing data to ensure that medications are safe and effective.

If you’re interested in working in a fast-paced environment where you’ll have the opportunity to contribute to something meaningful and make a difference in people’s lives—and you have a passion for data—a career as a pharmacovigilance scientist could be right for you.

Here are some tips and an example resume to help you write a fantastic pharmacovigilance scientist resume that hiring managers will love.

Jennifer Thomas
Chicago, IL | (123) 456-7891 | [email protected]

Highly experienced pharmacovigilance scientist with a proven track record in the pharmaceutical and biotech industries. Proven ability to identify and assess safety risks associated with the use of drugs and medical devices. Seeking a position in a company that values safety and innovation.

University of Illinois at Chicago Jun '10
Ph.D. in Pharmacology
University of Illinois at Urbana-Champaign Jun '04
B.S. in Biology
Company A, Pharmacovigilance Scientist Jan '17 – Current
  • Conducted pharmacovigilance (PV) data analysis and interpretation of safety reports to identify potential signals, including adverse event causality assessment; reviewed medical records for accuracy and completeness.
  • Developed a comprehensive understanding of the drug development process from preclinical through post-marketing phases by participating in project team meetings, reviewing documents such as study protocols, clinical study reports, etc., and performing literature searches on assigned projects.
  • Assisted with preparation of regulatory submissions such as INDs or NDAs by conducting scientific reviews of application content related to assigned projects and providing feedback regarding adequacy of documentation provided within applications.
  • Participated in internal quality control activities such as audits and training sessions to ensure compliance with applicable regulations/guidelines and company policies & procedures.
  • Provided support for external auditors during their site visits by preparing appropriate documentation required for audit engagement completion and assisting with any ad hoc requests that may arise during the course of an audit.
Company B, Pharmacovigilance Scientist Jan '12 – Dec '16
  • Assisted in the development of a new safety database for tracking adverse events and medication errors, resulting in improved patient care
  • Conducted pharmacovigilance activities on marketed products including post-marketing safety surveillance, epidemiological studies and spontaneous reporting analysis
  • Provided scientific advice to management regarding product risk assessment and mitigation strategies for marketed products
  • Developed training materials for all levels of personnel involved in pharmacovigilance activities
  • Analyzed data from clinical trials, epidemiological studies and spontaneous reports to identify potential risks associated with drug therapy
Company C, Clinical Research Assistant Jan '09 – Dec '11
  • Coordinated and conducted clinical research studies in compliance with federal regulations, institutional policies, and Good Clinical Practices.
  • Performed study visits with patients, collected clinical data, and ensured accuracy and completeness of data entered into the electronic case report form.
  • Monitored patients for adverse events and reported them to the Principal Investigator.
  • Certified Clinical Research Professional
  • Certified Regulatory Affairs Professional
  • Clinical Data Manager

Industry Knowledge: Biology, Chemistry, Pharmacy, Clinical Research
Technical Skills: SOPs, Good Manufacturing Practice (GMP), ICH, ICH Q6B, ICH Q10, ICH Q11, ICH Q12, ICH Q14, ICH Q15, ICH Q16, ICH Q17, ICH Q18, ICH Q19, ICH Q20, ICH Q8, ICH Q9, ICH Q10, ICH Q11, ICH Q12, ICH Q14, ICH Q15, ICH Q16, ICH Q17, ICH Q18, ICH Q19, ICH Q20, ICH Q8, ICH Q9, ICH Q10, ICH Q11, ICH Q

How to Write a Pharmacovigilance Scientist Resume

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

Write Compelling Bullet Points

Bullet points are the most effective way to showcase your experience and qualifications. And when it comes to bullet points, the more specific and detailed you can be, the better.

For example, rather than saying you “conducted research,” you could say you “conducted pharmacovigilance research on adverse drug reactions to identify potential safety concerns and develop mitigation strategies.”

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

Identify and Include Relevant Keywords

When you apply for a pharmacovigilance scientist role, your resume will likely 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 in the job description. If your resume doesn’t have enough relevant keywords, the ATS might not forward it to a recruiter.

To increase your chances of getting an interview, make sure to include relevant keywords throughout all sections of your resume. You can find a list of common pharmacovigilance scientist keywords below:

  • Drug Safety
  • Pharmacovigilance
  • Drug Development
  • Clinical Trials
  • Electronic Data Capture (EDC)
  • MedDRA
  • Computerized Clinical Trial Data Capture (CCTC)
  • Good Clinical Practice (GCP)
  • Oncology
  • Medical Writing
  • Validation
  • Regulatory Submissions
  • Clinical Pharmacology
  • Clinical Development
  • Pharmacology
  • Pharmacotherapy
  • Hospitals
  • Biotechnology
  • Good Laboratory Practice (GLP)
  • In vitro Clinical Studies
  • Oncology Clinical Research
  • Good Clinical Practice (GCP) Standards
  • Healthcare
  • Good Manufacturing Practice (GMP)
  • Biologics
  • Cell Culture
  • SAE
  • Clinical Research
  • Chemistry
  • SAS

Showcase Your Technical Skills

Pharmacovigilance scientists need to be proficient in a number of software programs and databases in order to effectively do their jobs. These might include adverse event reporting databases, clinical trial databases, and patient medical records. They also need to be able to use statistical software programs to analyze data.


Solar Designer Resume Example & Writing Guide

Back to Resume

RPO Recruiter Resume Example & Writing Guide