What exactly is pharmacovigilance, and why is it so crucial?

Pharmacovigilance strives to increase patient safety by conducting ongoing investigations, and identifying and monitoring previously unknown adverse effects, it is critical to ensure that any medicines developed and manufactured by pharmaceutical companies are effective and do not pose a serious risk to consumers. Pharmacovigilance is the science of collecting, detecting, assessing, monitoring and preventing adverse effects of pharmaceutical products. 

Pharmacovigilance Eligibility Requirements

1. Aspirants to pursue a professional career in Pharmacovigilance.
2. Graduate or postgraduate degree with at least aggregate marks.
3. Pharmacy or Pharmaceutical Sciences graduate or postgraduate degree.
4. Medical graduates and a bachelor’s degree in a relevant subject, such as life, health, or pharmaceutical sciences, are required.
5. When it comes to drug safety, the career path is very straightforward, in both perpetual and procuring capacities.

Skills required to start a career in Pharmacovigilance

Pharmacovigilance-Career Prospect

Young professionals are hired as a junior or an assistant before their functional job titles such as Junior or Assistant Project Manager. After gaining experience, the prefix can be changed to Senior Project Manager.

Many young scholars begin their careers in the pharmaceutical industry as employees, which then outsource them for a set period to a pharmaceutical company for a specific job. Then after, these young professionals will choose their future career development. 

Fresh graduates typically begin thinking about their career development in the pharmaceutical sector after a period of varying work experience. Whether you want to remain an expert in your field or become a manager or leader, each requires different skills, training, and work experience.

No matter what role or level of position, pharmacovigilance professions require excellent communication skills.

Pharmacovigilance is regarded as an excellent career option for those interested in a well-defined and expanding career path. There is a faster career progression leading to managerial and director roles eventually, as well as a decent salary package. The entry-level job for someone looking to start a career in Pharmacovigilance is that of a Drug Safety Associate. 

Progression to a more senior role, such as Team Lead or Director, which carries more responsibility and allows to manage teams.

Pharmacovigilance- Positions

Drug Safety Associate

• This is the entry-level position in Pharmacovigilance, and most students pursue it after studying Pharmacovigilance. 
• Drug safety associates are pharmaceutical, life science, nursing, or medical graduates who specialize in monitoring adverse drug effects in patients and reporting these effects for review and drug modification. 
• Drug Safety Associates are primarily responsible for case creation, data entry of all information available in the document, reconciliation, checking for minimum safety information, and the follow-up process. They will be required to submit reports to regulatory authorities. 

Drug Safety Scientist 

• Another important career option in Pharmacovigilance is drug safety scientist. After gaining years of experience as a DSA, a person can become DSS. 
• A drug safety scientist should have complete knowledge of medical coding, a good understanding of medical terms, and a general understanding of regulatory affairs.
• DSS’s job is to ensure that pharmaceutical products are both effective and safe. They oversee detecting and reporting adverse drug effects.

Aggregate Report Scientist 

The aggregate report scientist is the next step in the Pharmacovigilance career path. This entails compiling a drug’s safety data over an extended period. This position can be obtained after gaining good narrative writing experiences in individual cases, such as writing PADER.

• The purpose of a PADER report is to provide any new information obtained from the source medicine.
• It analyzes data to identify any exposure to the medicine.
• Compile information on the status of the medicine’s approval in various countries and regions.

PADER Technical Specifications

• It’s a single pdf file that includes the table of contents, bookmarks, and hyperlinks.
• A Study Tagging File (STF) is not required to submit PADER’s descriptive part in eCTD format.
• The reporting period is included in the PADER/PAER title, whereas the leaf title follows a standard format for future submissions.
• PADER supports hyperlinking, which will aid reviewers in understanding the document.

Sollers add value by providing a reference for appropriate fields. Let us work together to create a better future! Learn about Sollers Career Guidance.

• assistance is given – hands-on database and system training
• assist in achieving results – gaining extensive experience
• assistance with references
• assist in establishing necessary contacts
•  career advancement features

Sollers College offers Master’s, Bachelor’s, short-term programs, and certificate programs in Life Sciences. Clinical trial management, advanced clinical research, drug safety, and pharmacovigilance are the main topics of our courses. 

Sollers unique program always opens a wide range of career opportunities in the pharmaceutical industry and provides the right guidance for professionals with quick support for learning. 

Sollers offers training programs to students who are ready to build their profiles. 

Sollers designed a pathway to the vast pharmaceutical industry to learn and demonstrate your expertise. Don’t let yourself be held back in this pharma and drug industry to match your requirements.