Clinical Programming

Clinical research includes a broad range of disciplines such as:

– Clinical monitoring
– Project Management
– Data Management
– Regulatory Affairs
– Quality Assurance
– Pharmacovigilance
– Business Development
– Medical Writing
– Medical Affairs

Below is an outline of two job roles that are absolutely essential to clinical research trial.

Clinical Research Associate
The role of a clinical research Pharmacovigilance training  associate is to plan, carry out and analyse clinical trials. Clinical trials involve studying various aspects of a medical product. For example they might test for side effects, health benefits, potential risks and general benefits in order to asses whether a product should go to or be taken of the market. However, most tests must be done before a product is allowed to be sold in the shops.

There is a specific procedure for a clinical trial which determines whether a drug can be used on humans. The drug needs to be tested on healthy humans and then compared with patients that have symptoms that need to be cured. Clinical trials are also carried out after a product has gone to market to track potential side effects as some drugs work differently when used in the mass market. Some of the things that a Clinical researcher might be involved with on a daily basis are things like training new staff, completing administration tasks and record trial data, putting together final reports, communicating with doctors during a trial, checking safety procedures and designing data collection forms.

A clinical programmer is a very important part of any clinical project. They spend most of their time working with the clinical research team to analyze, organise data and manage databases. Some of the qualities that are valued by employers looking for talented individuals to take on this role include having an in depth knowledge of computers, the ability to write code and a degree in a related science.

It usually takes around 4 years to complete a degree in most related subjects such as Life Sciences, Pharmacology, Information systems or Nursing. On top of this, to become a Clinical Programmer you need to have around two years experience in pharmaceutical programming in a clinical research environment. This can be a very rewarding job when new and exciting results are produced and trials run smoothly and successfully.