If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
About The Company:
Winner of the ACRP-Avoca CRO Quality Award in 2018
Recognized with six CRO Leadership Awards from Life Science Leader magazine
Eagle Award winner - which recognizes outstanding leadership, professionalism, integrity, and dedication to advancing the clinical research profession through strong site partnerships
CRA is offered the unique opportunity to be involved at every stage of the drug development process by providing unrivaled support to our customers.
If you want an exciting career where you use your medical or health background and education, travel extensively and are instrumental in the clinical trials process, this could be the opportunity for you.
Our successful Clinical Research Associates possess varied backgrounds in the medical and related healthcare fields.
Individuals who have succeeded in the CRA role and comes in with at least 1 year independent monitoring experience.
An extensive training program provides the platform to effectively and confidently carry out your duties.
Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
Perform source document verification and case report form review;
Perform regulatory document review;
Conduct study drug inventory;
Perform adverse event and serious adverse event reporting and follow-up; and
Assess patient recruitment and retention.
We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.
- Please feel free to drop your resume at faiza. khan @ nesgt. com for more information/or detailed chat over the role Call 02-9696 8008.