A ‘clinical research coordinator’ (CRC) also sometimes referred to as ‘site research coordinator’ (SRC) or ‘study coordinator (SC)’ or simply ‘research coordinator’ is one of the most important person at a clinical research site and plays a very vital role in the conduct of a clinical trial. A good CRC with good understanding of the clinical trial processes, guidelines and regulations is a huge advantage to any clinical trial site. A CRC is the person who is regularly in touch with clinical trial subjects and conducts most of the study related procedures and documentation as delegated to him/her by the principal investigator… A CRC is a link between the sponsor / CRO, investigator site and the ethics committee. Thus, this job profile demands high competency and knowledge of clinical research. In order to start your career as a good CRC having completed a course in clinical research will be a great advantage and addition to your resume. An online post graduate diploma in clinical research from James Lind Institute will equip you will all the required skills and knowledge to stand a class apart from the rest of your industry colleagues. An online post graduate diploma in clinical research will allow you to study at any time and complete the course as fast as you can. This will give you an advantage to apply for higher positions in the clinical research industry with attractive salary packages and benefits.