Asmita Titre

Drug Safety Operations Lead at Qinecsa Solutions

Based in United Kingdom

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Seniority

Manager

Department

Other

Location

United Kingdom

Industry

Pharmaceutical Manufacturing

Company size

972

Contact information

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Email

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a•••••••@qinecsa.com

Phone

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+44 ••• •••• ••••

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Background

About Asmita Titre

I'm a Pharmacovigilance Leader who loves to play with Data, measures success by creating self-sustaining teams that deliver consistent results with constant improvising work culture to drive Pharmacovigilance operations smoothly. As a tenured PV Specialist with 8.3 years in Pharmacovigilance with 4.6 years in leadership capacity, I can collaborate and determine the best way to make an idea into a reality. I am looking forward for a trajectory role where i am responsible for management of projects and innovations, ensure optimum utilization of resources, make complex decisions, contribute as pharmacovigilance data science POC, pilots, project implementation, vendor management support, properly focused protocol designs and reported outcomes. In my role as a Team Lead within the CRO industry, I've cultivated a profound understanding of clinical research operations and adeptly managed teams. Beyond my clinical expertise, I've also been passionately involved in Data Science, where I served as a Data Governance Lead, overseeing a team of pharmacists for an online pharmacy platform. My extensive experience spanning 15.6 years, complemented by my Six Sigma Green Belt certification, reflects my commitment to tailored solutions for effective team and interpersonal interactions. As a highly motivated and results-oriented professional, I'm actively pursuing a Project Manager position with the goal of enhancing profitability and revenue, all while infusing a positive perspective into projects. I have additional interest in roles like RWE, HEOR, Pharma clinical analytics as all these are closely linked, as they are areas that involve the evaluation of drug safety and effectiveness. Pharmacovigilance managers can make use of HEOR / clinical analytics to evaluate the real-world safety and effectiveness of drugs, by analyzing data from clinical trials, post-marketing surveillance, and other sources. Overall, clinical analytics and pharmacovigilance are complementary areas of the pharmaceutical industry, and both are critical to ensuring the safety, effectiveness, and value of healthcare interventions. Both combined, pharmacovigilance managers can make become more cognizance of clinical data and its outcomes to make informed decisions about drug safety and effectiveness to ensure best possible option to the end user.

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