Tara Dougherty

Tara Dougherty is a Clinical Research and Regulatory Affairs professional with 5 years of experience in the Pharmaceutical and Biotechnology industries. Tara's strengths include negotiation, problem solving and benefit-risk analysis. Tara has specific expertise in Electronic and Paper Regulatory Document Management, Regulatory Submissions (i.e. Investigational New Drug, New Drug Application, Biologic License Application and the Electronic Common Technical Document or eCTD), Multiple Study Site Startup requirements and IRB liaison. Tara is seeking an opportunity where I can help bring high quality effective medicines to market while making them safe for the global population. Tara has additional experiences below:

• Advanced knowledge of US and EU regulatory submission requirements for investigational drugs (IND/IMPD/CTA) marketing applications (NDA/BLA/MAA) as well as proficiency in ICH guidelines for eCTD formatted submissions.
• Advanced degree in Regulatory Affairs from Temple University's School of Pharmacy.
• Critical thinker and problem solver with success in achieving and exceeding organizational and departmental goals and objectives.
• Strong written and verbal communication skills including experience giving presentations to various audiences both scientific and business knowledge.
• Strong computer skills including the use of Electronic Document / File Management Software and the ability to use the internet to research current and future scientific and regulatory trends.