Medical Writing
Medical writing includes the design and production of printed or digital documents, particularly about medicine or health care. It is also, an art of creating clear and precise scientific documents that includes clinical research documents, healthcare websites, fitness and medical journals as well as health-related news. Along with this, it includes documentation for clients of media industry, government, clinical research organizations (CROs) and medical device manufacturers. You can be a professional medical writer with clinical research courses and training.
Medical writing can be broadly classified into Regulatory
medical writing and Educational medical writing:
1)
Regulatory
Medical Writing :
Regulatory writing is a branch of
medical writing that
focuses on the documents that a medical
writer or a regulated medical writer must submit
to the regulatory authorities at various stages of a clinical trial. In general, each
country has its own national
authority that requires approval for the marketing and sale of pharmaceuticals, cosmetic products, food and
biological products.
These documents include clinical trial
protocols, clinical trial reports, patient consent forms, drug brochures, and the most important- Common Technical Documentation [CTD] in the prescribed format.
2) Educational
Medical Writing :
These documents are
intended for the general public and are written in basic, non-technical
language. This subset of medical writing helps create literature, journal manuscripts, and summaries of drug-related education and
distribution. Also, creating content for health-related
journals, newsletters, and websites is altogether the job of an
educational medical writer.
Education:
Earn a bachelor's degree in a related
science field. In fact, medical writing requires highly specialized skills.
Hence, most employers are looking for candidates with a degree in related fields such as life sciences or statistics. On the other hand, a bachelor's degree can be a good start to
your career.
What do medical writers do?
·
Medical
writers generally work closely with
scientists, doctors, and other subject experts to create effective documents that visibly define
research results and product usage.
·
Medical
writers write, proofread, and finalize
protocols, investigator brochures, outlines, regulatory documents,
and clinical documentation.
·
They must
ensure that the results of clinical or scientific
research and statistical interpretation are accurately reflected in the final document.
·
They
coordinate with clinicians, clinical
scientists, bio-statisticians, and pharmacists to interpret research
results.
·
Medical
authors certify that their medical documentation complies with the International Conference on Harmonization (ICH) or other relevant
regulatory guidelines. Medical
writers develop standard operating
procedures for preparing and maintaining
appropriate medical correspondence for their
company.
·
The medical record
transfer officer ensures that appropriate
documented quality control (QC) tests are performed on the medical transfer service.
·
Medical
editors work for companies that manufacture medicines and medical devices to design training and informational materials for kits and package inserts
used by doctors and nurses.
Job Opportunities:
Presently, careers in
medical writing are on the rise, and the
demand for medical writers is very
high. Medical writers can find work in niches such as:
·
Media & Publishing companies
·
Reputed Medical Journals
·
Academic medical institutions engaged
in providing education to healthcare professionals.
·
Medical/scientific societies.
·
Pharmaceutical/healthcare product
companies including medical device companies.
·
Healthcare Websites.
An effective medical writer for the patient is important because, it ensures that the audience
retains a high percentage of the information presented. A better understanding of the
patient leads to better information recall, patient satisfaction, treatment compliance, and improved health!
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