Manager Scientific Writing-Pharmacovigelence

The roles and responsibilities of the Manager Scientific Writing—Pharmacovigilance include the following:
· Developing scientific medical content for all projects that meet international quality standards
· Interfacing with clients on a regular basis to meet their expectations
· Controlling/reducing the cost of content development, cycle times, and error rates in projects
· Developing innovative medical content products by leveraging on the depth of scientific content
· Adhering to compliance procedures and internal/operational risk controls in accordance with any and all applicable regulatory standards, requirements, and policies
NOTE :
EDUCATION—MD/PHD/MBBS/MPHARM
EXPERIENCE—5-7 YEARS OF EXPERIENCE IN PHARMACEUTICAL COMPANIES IN ANY OF THE FOLLOWING FUNCTIONS: MEDICAL SERVICES/MEDICO-MARKETING/CLINICAL RESEARCH/REGULATORY AFFAIRS; MEDICAL WRITING/DEVELOPI