Brief Job Description: Clinical Research Associate supports clinical trial activities, carries out reporting and documentation for monitoring of research activities so as to ensure regulatory compliance and good clinical practices as per ICH and coordinates with site staff members, investigators, SMO and Sponsor/CRO.

Personal Attributes: The individual should have in depth knowledge of pharmaceutical drug development process, clinical trial related process regulatory requirement and scientific aspect of study. Individual must demonstrate, excellent communication skills, analytical and critical thinking, attention to detail, decision making and proactive planning and organizing skills.

NATIONAL OCCUPATIONAL STANDARDS 

1.  Support clinical trial activities

2.  Carry out reporting and documentation for clinical trials

3.  Maintain a healthy, safe and secure working environment in the life sciences facility

4.  Coordinate with team members and site