developing compelling technology-based business process solutions. Specific areas of capability need to be: Clinical Services Clinical Data Management BioStats & Statis Programming Safety Services Pharmacovigilance Complaints Management Regulatory Services Regulatory Operations Medical Writing Commercial Services Marketing & Sales Contract Management Solution Development Experience in developing solutions ground up, in partnership with more »
top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy & Operations as well as Quality and Safety (eg. Pharmacovigilance).As a Senior Consultant, you will manage complex and novel consulting projects for Veeva customers in the research and development (R&D) space – managing teams more »
be required to understand, cleanse, and present clinical safety data sets in an early stage/pre-marketing environment. Responsible for: Day-to-day pharmacovigilance oversight : Review SAEs and queries to investigators on a regular basis, support the data cleaning for safety data, and oversee signal management to identify significant … including interpretation of safety data from tables and listings. Consulting on process improvement: Support our ongoing data management transformation initiative, reviewing current processes for pharmacovigilance and safety risk management and providing input on transformation plans. Deliverables: Input to data management transformation initiative e.g. recommendations for Risk Evaluation and Mitigation Strategy more »
