In this busy world of the never-ending rat race, driving your successful career is a bit difficult. The way you emphasize your career growth may not be the same in actual cases if you don’t take the correct steps while choosing your career. As you see, the growth rate of many promising jobs is bait these days. Building a tremendous career path is indeed a game of its own rule. We need to be very careful while choosing our career.
As the pharmaceutical industry continues to thrive you need to move according to the landscape. The Drug Safety and Pharmacovigilance certification program is gaining huge attention day by day. This certification has an inherent potential to set your outstanding career path. Drug Safety and Pharmacovigilance play a vital role to ensure patient safety in terms of correct usage of pharmaceutical products. It should be there throughout the journey of drug development. It’s all about safety!! Ensure the timely detection management of expected and severe events and suspend unexpected adverse events.
This course is designed to attain the required skills and quality blended with a clear methodology to have steady growth in this field. In this program, you will be able to learn fundamental topics like Regulatory Compliance for Drug Safety and Pharmacovigilance, Risk Management, Signal Evaluation, Reports, Successful navigation of drug safety, pharmacovigilance as keys to product longevity, consumer confidence, regulatory compliance and more.
Based on the level of exposure you want your career progression can lean either towards in technical direction that includes epidemiology, risk management and signal direction or else in line management. The main objective of Pharmacovigilance or Drug Safety Scientist is to detect, evaluate and prevent the adverse effects of medicines and drugs. There is another role too to assess the products in terms of risk/benefit to ease the use of the product. As a Pharmacovigilance professional, you need to enter the event in appropriate databases, follow-up with the event to collect additional information and send these reports to regulatory authorities and other appropriate regulatory bodies.
In the initial stages, you tend to work as a drug safety coordinator or associate. Responsibilities include entering data of cases, capture drug identifiers, detailed event reports.
Once you gain 2-3 years of experience you will be designated as a narrative report writer to provide a summary version of event reports to enable the reader to conclude the event or work on medical coding. Mould your position as a Drug safety scientist or Clinical Drug Safety officer with this experience.
If you have good narrative skills, switch to write and review about Periodic Safety Update Reports (PSUR) or Development Safety Update Reports (DSUR) and also risk management plans or attain roles like Drug Safety Medical Writer. If your experience rolls on year by year your career path builds as a Team lead, manager, Associate Director, Director, Vice President progressively.
Plan wisely……..Act accordingly……..Access long term opportunities in shorter periods with Sollers Certification Program.