Clinical Research Associate Responsibilities

The following article enumerates the various responsibilities of a Clinical Research Associate in the various testing processes in the field of pharmaceuticals. The responsibilities of a Clinical Research Associate spans over a vast range but the primary function is the ability to conduct tests and trials of products on various subjects.

The significant role of a clinical research associate lies in setting up and monitoring such trials.

Clinical Research Associate Job Responsibilities

Must develop and design suitable methodologies for the trials.
Should have good communication skills as a Clinical Research Associate is responsible for putting forward the methodologies to a committee.
Coordinating with doctors and medical professionals on the conducting of the trials.
Must make sure the trial center is monitored on a regular basis.
Must maintain a record of all data and records of the trial.
Must have a good knowledge of existing laws and legal protocols involved in the testing and production of any new drug.
Must be able to train staff.
They are the essential communication line between the investigator and sponsor.
Is liable for the proper conduct and safety throughout trial.
They need to verify that investigator follow approved protocol & all the GCP procedures.
Along with this, they must verify the documents or source data & other trial-records whether they are maintained well, complete and accurate.

Category: Pharmaceutical Job Responsibilities