Do you want to start a promising career that allows you to help Canadians across the country stay safe and healthy? If you become a clinical trial and pharmacovigilance professional, you can do just that.
Professionals in this field are responsible for the safety of drugs and medical devices. They also make sure that clinical trials are conducted safely and adhere to proper protocol. By ensuring that clinical trials run smoothly, pharmacovigilance professionals help expedite the process of getting life-changing pharmaceuticals to market. These pharmaceuticals can make a huge difference in the lives of people suffering from disease, illness, or chronic pain.
Want more information about what you’ll learn during your pharmacovigilance training? Read on to discover three key skills you’ll develop.
1. In a Pharmacovigilance Program You Will Learn About Organizing Clinical Research
A good pharmacovigilance program will provide students with both foundational and practical knowledge so that they are well prepared to enter the workforce after graduating. One of the main skills you will develop is the ability to organize and monitor clinical trials. You will learn how to identify and evaluate work sites and labs for conducting trials, how to coordinate the participants of a clinical trial, and how to manage the budget of clinical trials.
Each of these components plays an important role in ensuring that clinical trials run smoothly. For example, budgeting is an extremely important skill because clinical trials can become expensive if budgets aren’t properly adhered to. In addition, many clinical trials are paid for by a sponsor. If the budget is excessive, the sponsor may not cover the cost of the trial.
2. You Will Learn How to Manage Data in Your Pharmacovigilance Program
The entire purpose of clinical trials is to collect data on the drug or medical device that is being tested. Therefore, developing strong data management skills is extremely important for students completing a clinical research diploma.
During your training you will learn about the role that data managers and data management associates play in clinical trials. These professionals are involved with trials from their very beginning to their very end. Data managers help determine the best way to collect data, then oversee procedures to ensure it’s collected accurately, timely, and on budget. Data managers also act as a liaison between different bodies collecting data, such as the laboratory that tests samples and doctors who record their observations.
Throughout your training you will learn how to develop a sound data management plan and oversee data collection. By the time graduation comes, you will feel confident in your ability to design, prepare, and implement a great data management plan.
3. You Will Learn How to Write Reports During Your Pharmacovigilance Training
Being able to create reports that accurately depict the progress of a study is an important skill for pharmacovigilance professionals to have. During your training you will learn how to write a variety of clinical research reports, such as safety reports, study reports, and more.
These reports are extremely important. Drug development companies can be required to release reports about drug safety during the development process or even after a product has made it to market. Ensuring that the content within each report is accurate and easy to understand is crucial and could have a direct impact on an individual’s health.
During your clinical research training, you will learn about reporting
The skills you will learn during your clinical research program are extremely valuable to employers. Knowledgeable pharmacovigilance professionals are in high demand across the country, and that demand is growing. Your knowledge of clinical research reporting will be a great addition to your resume once you begin your career.
Are you interested in enrolling in clinical research courses in Toronto?
Contact AAPS today to learn how you can get started.
1-855-502-2288