i) Literature articles / Write-ups.
Checking the Marketing material like Visual Aids, Leave behinds etc. for medical authenticity.
Answering the field queries.
Preparing New drug proposal.
Conducting Training sessions for BO’s & Marketing dept. on existing & current products.
Current product launch: Training slides, Manual, Monographs, PIs and ABPIs
Collection and updation of the latest information available of the existing products.
coordinating with the investigator etc).
Assisting in submission of documents to the Ethics committee.
Monitoring the trial & trial related documents (in office & off- site).
Statistical Analysis.
Report Writing & Publication.
III] REGULATORY
Preparation of required documents (Rationale).
Literature support for regulatory queries.
Justifications for product combination.
For Regulatory submission Co-ordination and obtaining all the doctors required for DCGI submission- CRDs, R& D and Regulatory.
IV] TOXICOLOGY STUDIES
Vendor selection, study startup, Timeless monitoring, report reviews and payment.
V] TRAINING TO TEAM MEMBERS
📌 Medical Advisor Maharashtra
🏢 Zuventus Healthcare
📍 Maharashtra
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