Clinical trial assistants (CTA’s) usually work in administrative positions to assist with the process of a clinical trial. Clinical trials are research studies that determine whether or not a new medical treatment such as a drug or device, is both safe and effective for human use. These intricate studies are required by law and are used to show how certain medical approaches are perhaps more effective to treat specific illnesses than others. The need for a CTA is amplified during these studies because trials are often highly monitored and regulated. This means that a great deal of intricate record-keeping is necessary and all of this must be in accordance to compliance.
A CTA takes the burden off and relieves a lot of the pressure associated with this side of a clinical trial. Most CTA’s, as mentioned above, act as support staff. However, it is not unusual for one to take on some medical duties such as performing lab tests or taking a sample of blood, for example.
Computer and Administrative Work
One of the main reasons why people hire a CTA during a clinical trial is because they are more qualified to deal with software applications such as PowerPoint, Excel and Word. Researchers may not have the time of expertise to deal with this side of the trial, which is where a CTA comes into the equation. They usually have excellent computer and administrative skills which helps them with such tasks. In addition to this, a qualified CTA will show exceptional written and verbal communication skills as well as showcasing a degree of medical office management experience.
Sufficient Education and Training
CTA’s must be qualified with an associate degree in a field of health and science etc. An academic background is a plus in this field of work, especially if they have experience in pharmacy or health care management for example. Having qualified and professional Clinical Trial Assistants, such as those provided by gandlscientific.com, will help to ensure your trial runs as smoothly as possible.
Strong database skills are necessary because you will be relying on your CTA to maintain, manage and update site demographics on computer databases. This takes a huge workload off your back, allowing you to focus on the trial at hand. It is up to the CTA to gather important data, log clinical research forms and to transfer data when necessary between different forms in accordance to the needs of the trial.