To People Who Want To Start Pharmacovigilance Writing But Are Afraid To Get Started

Medical writing is a wise career option for all those who have a knack for writing and are into science. The recent years have seen an escalating demand for medical writers and pharmacovigilance is one such segment of it, which is gaining extreme popularity.

Science had developed with a great pace and advancements have been made into the medicine sector. Various new drugs are being developed for the treatment of various diseases. With the rapid inventions of new drugs, the question of the safety and efficiency of the drugs remain persistent. Pharmacovigilance tends to answer this question.

Pharmacovigilance writing:

Pharmacovigilance writing deals with every aspect of drug development. It starts with the clinical trials continuing with submission of essential reports prior to the market authorization of the drug and goes forward till the post marketing of the drug.

Skilled writers, who can put in the efforts and expertise in clinical development and various technical aspects into the various related documents, to make the documents authentic and in accordance with the guidelines.

When going through the clinical development stage, a drug is required to have accurate reports on the safety and efficacy in the trials. The adverse effect of the drugs and the safety levels are measured from the reports from trials.

Benefit-risk regulatory reports are the key document/feature for a pharmacovigilance writer. They write the analysis of the safety and efficacy of the drug with an aim to bridge the gap between healthcare professionals and public in general enabling patients to develop a trust for the drug.

To be precise, pharmacovigilance writers contribute in the clinical drug advancement by giving inputs using their expertise in developing the clinical plan outlines and structuring clinical drug advancement programs for developing the drugs for the use of masses.

Why choose pharmacovigilance writing as a career?

More and more clinical researches are being conducted today. Pharmacovigilance counts for an integral part of clinical researches. Various pharmacovigilance organizations are working on drug safety control. The pharmacovigilance systems are facing a major human resource crisis and there is a lot of demand for the pharmacovigilance writers who can work on various clinical documents focusing on the safety and efficacy of drugs and help in the various documents related to the drug development process.

New drugs take time to reach the market as before they are out for sale in the market for the patients to use, they have to go through strict trials wherein their safety and adverse effects are measured and compared with that of their efficacy and efficiency levels and it is analyzed whether or not the drug is capable of treating the desired ailment and if it is worth taking the risk, I.e. the ratio of risk is to benefits is compared and then further decisions are made. The drugs must go through certain regulatory phases to achieve the ultimate goal of market authorization.

Seeing the current demands for the pharmacovigilance writers considering the significance of pharmacovigilance in the clinical and medical sector, it is a wise option to go for pharmacovigilance writing.

Pharmacovigilance writers can find work at:

• Pharma companies
• Contract research organizations
• Regulatory organizations
• Government regulatory agencies
• BPOs & KPOs
• Site management firms
• Regulatory consultants

How to ensure a successful career in pharmacovigilance?

If you are among those people who want to establish themselves into the field of medical writing but are concerned about how to start, this post helps you resolve your concern. Turacoz Skill Development Program offers 6-month diploma course in pharmacovigilance medical writing, where the individuals are made to understand everything about this sector, starting from the basics to the advance course.

This diploma course is targeted towards providing industry’s practical perspective in clinical research, drug advancement, documentation during drug development procedure, drug safety and various pharmacovigilance skills required in the industry. The motive behind this course is to make a successful pharmacovigilance professional.

The scope of this course is not just restricted to domain-specific training, but also involves personality development. Turacoz Skill Development Program offers various other courses such as regulatory writing course, freelance medical writing course, scientific writing, etc.

To know more about the courses, you can write us at trainings@turacozskilldevelopment.org

To register for the courses, click here.

Planning to be a freelance medical writer? Here is what you need to know.

Having a career as freelance medical writer is a good option indeed. But what you need to know is that there is no easy alternative to become a freelance medical writer. You will have to keep in account ‘n’ number of things.

You need to maintain a focus on the core specificities required for the job and will need to formulate a proper plan and decisions that will precisely reflect your medical/health writing goals.

From creating a portfolio to setting your rates, there is a lot of homework to be done before you jump start your career in freelance medical writing.

What is freelance medical writing?

As the name suggests, one has freedom of working from his/her desired location and can work for multiple clients and various medical documents at a single time, working as a freelance medical writer.

There is not going to be a fixed income, it all depends on how much you work and what rates have you set for yourself.

Stepping onto the freelancing dais:

You will be required to be well-off with these traits to begin with:

• Have a love and passion for writing
• Strong research and literary skills
• Being a Grammar-Nazi will certainly help you
• Knowledge of medical terminologies (will ease the work for you)
• A degree in life sciences or any medical field (though not mandatory)

Now that you know that you possess the basic skills required to start your journey, let's move towards another steps:

Creating a portfolio: If you have previously worked as a freelance medical writer or even as medical writer for any organization, you need to maintain a portfolio of your work. This helps your clients to know and assess your work and this will help you in getting projects. Showcasing your skills is the best way to get projects from different clients.

Choosing the right freelance websites: There are many websites that let you hunt for freelance medical writing projects. You need to choose the website you need to make an account on and look for projects. Go for more established websites. Some of such websites are:

www.upwork.com

www.peopleperhour.com

www.writersdepartment.com

www.freelancer.in

www.freelancewriting.com

Setting your rates: This is a very crucial element for a freelancer. If you are an experienced writer, you can create an impressive portfolio and showcase your work experience and set rates accordingly. For the beginners, it is always advisable to look for the rate other freelancers in the market have set and then fix yours accordingly. The competitive pricing strategy here is going to help you. Clients may consider you for lower price, but then keeping too low rates might also harm you. So, keep a hawk’s eye on the price other freelancer writers have set and analyze what rate would be safe for you.

You can also make your own website and upload your sample work there and create a good portfolio. You will need to learn the basic of making website or you can also hire a professional to make one for you.

Familiarity with basics of digital marketing: familiarity with SEO, SMM, etc. Will give you an added advantage when it comes to promoting your website and content.

The art of selling: Being a freelancer means that you have to play various roles and one of them is being a marketer. You need to market yourself as a medical writer. You need to convince the clients why you are better than others for a project.

Being a freelance medical writer comes with its own set of challenges:

• There is no fixed salary (deal with it!) you will earn as much as you work
• No added bonuses like medical insurance, provident fund, etc.
• Managing everything by yourself like maintaining accounts, keeping a track of your clients and their work
• Self-discipline is highly required as you will be monitoring your work on your own
• Self-understanding of the work becomes very important and you need to be clear about what client wants as there will be no one to guide you

Some advantages you can get as a freelance medical writer are:

• Working from the comfort of your home
• Chance to work on variety of documents
• Opportunity to work for multiple clients and projects at a time
• No hassle for daily commute
• Personal space
• Better work-life balance

Want to know more on how you can build your career as a freelance medical writer? Contact Turacoz Skill Development Program (TSDP), a learning platform oriented towards establishing efficient medical writers and help them in achieving their goals.

TSDP offers a variety of medical writing courses with an aim to train writers as per the industry standards and help them in staying updated on the recent trends and make a successful career in medical writing.

To know more, you can get in touch with us at:

trainings@turacozskilldevelopment.org

Turacoz Skill Development Program helps you in achieving your endeavors.

Medical writing made easy for you! This article is the answer to all your queries regarding Medical Writing

A career in medical writing is indeed a very lucrative option. Medical writing is the best for ones who know how to put their literary skills to use and have the knowledge of therapeutic domain. Starting off as a medical writer might not be that easy but, then, it’s not even that difficult as you may think.
Everything demands some efforts. If you need to see favorable results, you need to work upon your goals first and then you’ll pass with flying colors. There are many of us who want to be a scientific writer or regulatory writer, but we hold back ourselves thinking of how to pursue this field.
Well, knowledge of science and medicine can certainly give you an edge, but you still need some extra skills to get medical writing career work for you. The medical writing courses with Turacoz Skill Development Program help you chase your dream of being a medical writer.
You might not be from a medical background, but you can still make it into this field. All you need is writing skills, research aptitude and knowledge of science. The medical writing courses offered at Turacoz Skill Development Program (TSDP) help you achieve your goal.
TSDP has a wide range of courses to offer, which includes:
6 months diploma course on medical writing and pharmacovigilance
TSDP offers this course in collaboration with Chitkara University, Chandigarh. The course is intended to provide industry insights on:

• Drug advancement
• Clinical research
• Documentation for drug development process
• Generation of various medical writing documents
• Drug safety and pharmacovigilance skills

The course is designed with blended technology mode, making it easier for the candidates to learn and have access to learning material anywhere and at any point of time.
The course also takes up personality development and resume writing, with an intention to groom an individually personally. The focus is to make students understand how to land a job and develop an understanding of the basic scientific principles related to regulatory writing, pharmacovigilance and publication.
Certificate course on scientific writing and conference presentation
To be able to write for a publication, one needs to be organized, clear, original, pragmatic, ingenious and precise. This course helps the students build an insight about scientific writing and different approaches to publication writing, distinct guidelines, peer-review procedure, publication ethics and essential tools for article submission.
Individuals looking forward to work in a publication in the medical field can join this course.
Regulatory medical writing course
Regulatory writing counts as the most crucial element of pharma domain. The rapid advancements in science and medical field has led to generation of various scientific and regulatory documents. These documents play an important role when the companies need to get approval for their drug/device from the regulatory authorities.
A regulatory writer is required to work on various regulatory documents like informed consent forms, investigator brochures, protocols, Common Technical Document (CTDs), etc.
TSDP provides basic and professional regulatory writing training. The tenure of the course is for 4 months and it is designed keeping in mind the recent industry and regulatory guidelines and focuses on building a skilled professional.
Want to know more about us and our courses? You can visit us here. For any course-related or other queries mail us at:
trainings@turacozskilldevelopment.org
We are constantly working towards bridging the competency gap and shaping the career of students by making them industry-ready.

Your Guide to Regulatory Medical Writing

Toiling over the test tubes on a jumbled lab seat is regularly just half the tale of scientific research. Having a lab book brimming with splendid outcomes will just prompt Nobel Prizes (or on a more ordinary dimension, continuous financing) if the data is scattered among the more extensive scientific network.

The sheer volume of results created in the improvement of a new medication is usually incredible for a pharmaceutical organization. It makes it impossible to review without anyone else's input, especially when review articles, conference reports, and other literature all must be set up altogether for the organization to advance their product successfully and morally. 

This is the where proficient communication organizations assume an imperative job. A typical interpretation is given to the job title of a medical writer, i.e., the creation of manuscripts for peer-reviewed journals.

There is another component of medical writing i.e., regulatory writing that has remained generally concealed. Each nation has its own governing body which grants approval to a drug prior to its release in the market. So as obvious by its name, regulatory medical writing deals with the composition of regulatory documents.

A regulatory medical writer uses his knowledge of science and research abilities to present the information and summarize the statistical findings. He oversees producing a variety of clinical documents throughout the complete life cycle of drug development, which includes the following array of tasks:

• Characterizing & reporting data from clinical trials
• Exhibiting the data accumulated by clinical trials
• Composing regulatory submission documents for regulatory authorities

An efficient regulatory writer is immersed into a wide range of tasks. They are well equipped to make a deal with the global regulatory imperatives, analyzing documents in clinical research procedure like Statistical Analysis Plans (SAPs), Good Clinical Practice (GCP) guidelines and Risk Evaluation & Mitigation Strategy (REMS) documentation.

The road to regulatory medical writing:

If you want to head into the world of medical writing and establish yourself as an efficient regulatory medical writer, there are a few perquisites that need to be looked after. Education is your main step towards anything and relevant, most importantly.

So, if you are planning on becoming a regulatory writer, you need to have:

• A degree in any stream of science like biology, microbiology, pharmacy, etc.
• A PhD in life sciences (though not mandatory)

It is not mandatory to be from a medical background, but it would be beneficial for one to be as it eases the process of understanding the complexities of science and write better.

Regulatory writers are hired by:

• Pharmaceutical companies
• Clinical Research Organizations
• Health authority regulatory
• Medical Communication firms
• Healthcare journals & websites 

The demand for medical writers is increasing rapidly in pharma and healthcare sector. a medical writer can work for any of the above-mentioned organizations or can also work as a freelancer. You need to have the right skills to break into the industry.

Breaking into regulatory medical writing with Turacoz Skill Development Program:

Turacoz Skill Development Programs focuses on building up the skills of aspiring writers and enhancing the ones of professionals too. It offers a wide range of courses related to medical writing, which helps an individual to break into this industry and have a dream start.

The courses offered are:

• Regulatory medical writing course
• Diploma course on medical writing & pharmacovigilance (6 months)
• Certificate course on scientific research & ethical consideration
• Certificate course on freelance medical writing
• Certificate course on scientific writing & conference presentation
• Trainings for academic institutes

All the courses mentioned above are designed with an aim to bridge the competency gap and enhance the skills of the writers. The courses are imparted by experts and professionals of their respective fields and focus is laid on the overall development of the individuals and to make them industry-ready.

The continuous assessment makes it easier for the writers to track their progress and improve.

You can reach out to us here for further details and register at trainings@turacozskilldevelopment.org

We are always ready to guide you in your endeavors.