Clinical Research Executive
Stipend: 8-15 KPM
Perform Site Identification and conduct Feasibility Studies.
Perform Site Selection Visit, Site Initiation Visits in accordance with the protocol and other applicable regulatory guidelines including local regulatory guidelines.
Send Follow Up letters to sites and submit Visit Reports to the Clinical Team Leader / Project Manager as required.
Keep a close association with site(s) for Patient Recruitment, Patient Follow Up, and protocol-related activities.
Training of Investigators on Protocol
CRF retrieval as per the project instructions.
Coordinate and distribute Clinical Study Material to study sites.
Archival of study documents.
BSc, MSc (Microbiology/Biotechnology), BPharmacy/MPharmacy/PharmD, MBBS, BDS, BHMS, BAMS, etc. and life science graduates
Clinical Research, a side stream of life sciences caters to extensive research carried out on humans either those who are in the pink of health or those who are battling life-threatening diseases. Currently, Clinical trials are emerging as a significant activity in India as it is vital to follow the drug and development programmer of the country. The only way to evaluate a new medicine is by implementing a well-designed clinical trial procedure. Moreover, clinical trials offer innumerable benefits to the participants. In addition to these evaluations, it needs to be ensured that there is compliance with the regulatory norms and proper training of concerned personnel.
The hype that is trending in India regarding clinical trials is perhaps an exaggeration of facts. However, these points to the necessity for ensuring compliance with the regulative norms and correct coaching of involved personnel in good clinical practice (GCP). By implementing these compliances, it will be ensured that India will reap the benefits of clinical trials and also become a world leader in this field.