SYNGENE Career Opportunities: Senior Executive - Medical Writing M.Pharm / M.Sc Apply Now
Job Purpose:
To develop and finalize clinical
and scientific documents related to medical writing, with a focus on
bioanalytical report writing
Key Responsibilities:
Independently develops and finalize
clinical and scientific documents including bioanalytical report, eCTD modules
and scientific communication documents
Performs literature search/review
as necessary to obtain background information for developing scientific content
Collaborates with internal and
external clients to support and enable effective communication resulting in
operational excellence
Ensure compliance to applicable
regulatory guidelines, department SOPs, client style guides, conventions as
applicable and deliver quality projects in agreed timelines
Creates and maintains SOPs and work
instructions for preparation and maintenance of compliant medical/scientific
writing deliverables
Ensures that appropriate documented
quality control (QC) checks are performed on medical writing deliverables and
responds to findings
Review of drafts including content
review, QC, and editing of drafts and final documents prepared by other/junior
team members before sharing with internal and external client
Follow any other instructions and
perform any other related duties, as assigned by the supervisor.
Follow environment, health, and
safety (EHS) requirements at all times in the workplace ensuring individual and
lab/plant safety
Attend training on environment, health, and safety (EHS) measures imparted company.
Educational Qualification:
M.Pharm / M.Sc
Technical/functional Skills:
Knowledge Bioanalytical procedures
and report writing
Preparation of eCTD document s for
regulatory submissions (Microsoft office and Adobe familiarity)
Good command on English language
and grammar
TO APPLY CLICK HERE
No comments:
Post a Comment