Ability to work in an ambiguous environment and produce maximum results with minimum direction and guidance. Demonstrated history of building and maintaining positive relationships both internally and externally.
Support data collection for regulatory and internal reports by compiling and reconciling data from multiple source systems and reporting tools within organization.
The incumbent will be responsible for Latin American countries through strategic market expansion, partner development, portfolio enhancement, and commercial excellence. Business Development & Revenue Growth. CORONA Remedies
experience in Drug Safety/Pharmacovigilance, including in post-marketing safety, with demonstrated expertise in aggregate reporting, safety surveillance, signal management, safety labeling, benefit-risk assessment and risk management is required.
A masters degree and/or PhD in Life Sciences e.g. Pharmacy, Medicine, Veterinary, or Biological Sciences, combined with experience working within pharmacovigilance and medical writing
Bachelor or Master Degree -MS/MA- Science Field. Support protocol amendments, Investigators Brochure updates, and Informed Consent Form revisions. Maintain Trial Master File, TMF and ensure timely filing and quality control of essential documents