The job of a clinical research associate is either full time or it is out sourced. Their role is to work directly with the research department of the pharmaceuticals. They are responsible to create case reports, enter clinical data, and provide content that is in compliance with the regulatory authorities.
Relevant licenses and certificates related to this field are required to apply for this job. Basic physical abilities to stand, sit, and walk are required.
Role of a Clinical Research Associate
They are responsible for managing the investigator sites with regard to health care and clinics. They are also responsible to adhere to the guidelines that are followed by the regulatory authorities at a local as well as a state level.
They are responsible to research and analyze these sites and provide corrective measures. The role could also be home based and these professionals can also work from home, based on this requirement.
Writing the Research
It involves developing templates and protocols that fit the writing methodology of these documents. They are also responsible to present these protocols to the committees in the medical and health care departments. They also require designing collection forms for data collection. They are also required to coordinate with the committee that deals with code of ethics and safety of clinical trials.
Liaising and Conducting Trials
These professionals are also required to liaise with doctors, medical consultants, and any professional of the medicine and health care. They are also meant to document patient data and verify for its accuracy.
They are also responsible to collect patient and other clinical data from hospitals. They sometimes also have to prepare medical and clinical manuscripts for publications.
Different certifications may be necessary to apply for this job. It depends on the company policy and their requirements for the suitable candidate. Click here for more details on Advanced Clinical Research Program.