Select a Region North America

Expertise

Haritha Sama

Director, Automation CoE

Expertise:

Haritha is a highly accomplished and forward-thinking professional with a proven track record in healthcare IT consulting and project delivery management within the healthcare and pharmaceutical industries. With a strong belief in technology’s potential to revolutionize healthcare, she is committed to harnessing data analysis, automation, and ML/AI to foster innovation and enhance patient outcomes.

Over her 13+ years at EVERSANA INTOUCH, she consistently delivered impactful results across various roles, leveraging her profound understanding of healthcare processes and technological expertise. Haritha is driven by her passion for streamlining workflows, boosting operational efficiency, and enabling clients to excel by offloading repetitive and data-intensive tasks to computers.

Presently, she plays a pivotal role in the Innovation team, spearheading the development and implementation of cutting-edge solutions. Collaborating closely with diverse teams, stakeholders, and clients, she identifies market needs, formulates product strategies, and ensures seamless execution from ideation to launch.

Throughout her career, Haritha has effectively managed products that have significantly benefited clients, driving cost reduction and operational efficiency enhancements. Her strategic thinking and adeptness at adapting to dynamic environments have been instrumental in fostering innovation and attaining organizational objectives.

Articles by Haritha Sama

Q&A: Enhanced Protection and Consistency for PRCI in Canada

Introduction At EVERSANA, we’re at the forefront of regulatory work in Canada, and recently, our team has been delving into the realm of PRCI (Public Release of Clinical Information) in  Canada and submission Policy 0070 (Regulation EMA (EU) 536/2014) in Europe). Understanding PCRI What is PRCI, and Why Does it Matter? PRCI stands for Public Release of Clinical Information, a mandate in Canada. In Europe this requirement falls under the broader Clinical Trial Regulations (CTR). These requirements compel pharmaceutical companies to publicly release all clinical information used in the drug submission process after regulatory approval. This information, often comprising hundreds of thousands of pages, is made available to foster innovation, […]

Interested in scheduling a meeting or speaking event?

お問い合わせ