The Associate position will involve data monitoring, data authoring, content development, maintenance & operations related to regulatory consulting projects. Individuals would get exposure to Clarivate-owned Life sciences databases and external data sources. The team is highly skilled, close-knit, and works towards a common goal of delivering quality projects to our global clients in life sciences industry.
We are looking for a Associate to join our Clinical and Regulatory Team in Hyderabad or Bangalore. This is an amazing opportunity to work on regulatory consulting projects. The team consists of six colleagues and is reporting to the Manager. We have a great skill set in data monitoring, content writing and consulting for multiple domains- regulatory submissions, clinical trials, marketing authorization applications (MAA), chemistry manufacturing and controls (CMC), CMC variations, pharmacovigilance projects, and regulatory strategy, among others, and we would love to speak with you if you have any of the skills or expertise in the regulatory affairs and consulting domain.
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