Work as Senior Clinical Research Associate at Covance

Pharma courses

pharma courses



Experience
• Minimum of four (4) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)
• In lieu of the above requirements, candidates with > four (4) years supervisory experience in a health care setting and three (3) years clinical research experience in the pharmaceutical or CRO industries (including monitoring) may be considered
• Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
• Excellent site monitoring skills
• Excellent study site management skills
• Excellent registry administration skills
• Ability to work with minimal supervision
• Good planning and organization skills
• Good computer skills with good working knowledge of a range of computer packages
• Excellent verbal and written communication skills
• Ability to train and supervise junior staff
• Ability to resolve project-related problems and prioritizes workload for self and team
• Ability to work within a project team
• Works efficiently and effectively in a matrix environment

Additional Information
Experience : 4 years
Qualification : University/college degree
Location :
Gurgaon
Industry Type : Pharma
Functional Area : Clinical Operations
End Date : 5th July, 2018

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