Expectations of a pharmaceutical applicant

Those who wish to pursue a career in the pharmaceutical industry are required to have a medical degree or an equivalent qualification in life sciences, nursing or pharmacy. Further studies such as postgraduate qualifications can be advantageous for a candidate wishing to pursue a career in the industry.

Some institutions of higher education offer a Master’s degree specialising in Pharmacovigilance, which is highly valued by many employers within the pharmaceutical industry. The course will provide students with vital knowledge and understanding of what a career in the industry entails, including experience of risk assessment, report writing and signal detection. Students also learn about existing regulatory authorities.

Experience is important when getting ahead Pharmacovigilance course of other candidates fighting for a position in drug safety and Pharmacovigilance. Observing and partaking in the industry first-hand as a placement student, or even shadowing a nurse or pharmacist demonstrates an applicant’s interest and willingness to work in a clinical background.

Careers in Pharmacovigilance

There are many different roles and job titles in regulatory affairs. Employees would typically begin their career as a drug safety associate, scientist or coordinator with sight to advance to specialty, senior and management positions in a particular area of Pharmacovigilance.

Medical writing, quality assurance and medical affairs are some of the main areas of focus for advanced employees; however these positions come with increased responsibility and require experience.

Also if candidates are willing, there are many opportunities abroad focusing upon drug safety. These tend to be positions in larger companies and so offer further scope for progression into authoritative roles.

The yearly salary for a career in Pharamcovigilance can vary substantially, but earnings usually fall between the figures of £25,000 and £60,000 per annum. This depends greatly on factors such as the regulatory body, location, experience and position of responsibility.

Types of jobs in the pharmaceutical industry

Drug safety officers are responsible for tracking and observing reactions and effects during drug trials and studies. A report on the study is to be submitted to regulatory authorities, and once the report has been submitted drug safety managers must organise and review the reports to monitor the profile of specific medication products.

Drug safety physicians assess and attain information about the safety of the products. They are also required to carry out medical case reviews and evaluate product safety during clinical trialling.

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