Prepares, literature review, abstracts, posters, and slide sets, and Manuscripts (complex) working from various data sources including clinical study reports, patient profiles, protocols etc.
Performs quality control (QC) checking / proof reading of the above mentioned deliverables to meet customer expectations.
Follows and tracks clinical trial milestones for assigned projects.
May act as liaison between publishing teams to ensure timely delivery of final documents for publishing.
Delivery of high quality clinical and safety documents in time and in compliance with internal and external standards
Act as an expert in the field of medical communication or medical information for the assigned Therapeutic area.
Assist the assigned scientific communication team in conducting comprehensive publication-needs analysis
This individual will have demonstrated expertise in partnering with clinical research, regulatory affairs, quality/reliability, product development, and bio - statisticians to develop schedules and timely execute tasks.
The individual will have demonstrated the ability to develop solutions to complex problems and ensures that solutions are consistent with objectives
Complies with and support group s project management tool, standards, policies and initiatives
Maintains records for all assigned projects including archiving. Maintains audit, SOP and training compliance.
Design an overall plan of action basis end-customers feedback & improve course content , customer management tactics and delivery.
Should have knowledge in clinical research and scientific writing.