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Associate Principal Engineer

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Dynamic IT Quality Manager with extensive experience at Alivus Life Sciences, specializing in GxP compliance and computer system validation. Proven track record in driving continuous improvement initiatives and ensuring data integrity. Adept at cross-functional collaboration and implementing ITIL processes, fostering a culture of quality and compliance across teams.

Business professional with 25 years proven track record in driving organizational growth and enhancing operational efficiency in diagnostics. Known for strong focus on team collaboration and achieving results in dynamic environments. Recognized for strategic planning, financial oversight, and adaptability with deep understanding of diagnostic technologies, lab operations, R&D, with understanding of global and local regulatory framework.

Creative Senior Program Manager with exceptional background in IT industry. Proven success building and motivating program teams to meet project goals. Demonstrated leadership in systems implementation, program execution and process improvement engagements.

Staff/Principal Software Engineer with 9+ years building cloud-native, scalable platforms in Java, Spring Boot, microservices, REST, and distributed systems. Led modernization from monoliths to microservices serving 2M+ users, boosting report performance 40%, cutting downtime 30%, and accelerating releases 50% via CI/CD and end-to-end observability. Deep expertise in API design, event-driven architectures, data integration/analytics, and enterprise security (OAuth2, JWT, SSO, RBAC). Cloud and DevOps across AWS/Azure/GCP, Docker/Kubernetes and Terraform/Cloud Formation. Known for driving adoption (+60%), reliability (+80%), and fast resolution of critical issues; seeking a Principal Software Engineer role to lead architecture, scale, and measurable business outcomes.

Diligent Senior Medical Coder with comprehensive expertise in medical coding and documentation. Successfully implemented coding accuracy initiatives that enhanced billing processes and compliance. Demonstrated proficiency in ICD-10 ensuring precise and efficient coding practices.

Dynamic People Leader with over 9 years of experience enhancing organizational performance through operational efficiency and talent development. Expertise in leading cross-functional teams, building stakeholder partnerships, and utilizing data analytics to drive strategic initiatives. Proven track record of translating enterprise objectives into actionable plans that consistently exceed targets and foster long-term growth.

The roles and responsibilities of Subject Matter Expert /Operations Lead entail overseeing and managing the team, ensuring that every member works to their fullest potential and delivers their assigned tasks with the highest proficiency. The duties of a leader also involve setting goals, assigning tasks, providing direction, coaching the team members and resolving conflicts.

Experienced Pharmacovigilance Professional with a keen eye for detail and knack for improving drug safety protocols. Known for enhancing compliance and ensuring patient safety through thorough data analysis and risk assessment. Proven ability to collaborate with cross-functional teams to implement robust safety protocols. Known for fostering collaborative environments and driving continuous process improvements.

Pharmaceutical professional committed to patient safety and regulatory adherence. Expertise in identifying adverse drug reactions and mitigating risks, ensuring compliance with industry standards. Reliable team collaborator focused on delivering consistent results and adapting to evolving regulatory requirements. Proficient in data analysis, risk assessment, and report generation. Eager to contribute to efficient contract management and project success.

I have 14+ years of relevant experience in aggregate report writing. I have experience in writing and reviewing Periodic Benefit Risk Evaluation Reports (PBRERs)/Periodic Safety Update Reports (PSURs), Monthly Signal Reports (MSRs), Risk Management Plans (RMPs), Risk Minimization measure (RMM) and Ad-hoc Reports. Additional reports that have written by me include ACO, Clinical Overview addendum, Health Authority Response and Reference Safety Information. Safety Trigger search from Non-EEA website (Australia, Japan, New Zealand, India and WHO). Handling a Trackwise project.
Proactive manager with demonstrated leadership abilities, strategic planning expertise and problem-solving acumen. Assists senior managers with accomplishing demanding targets by encouraging staff and coordinating resources. Methodical and well-organized in optimizing coverage to meet operational demands.

S S L Jayanthi Pokkuluri

Summary

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Drug Safety Associate

Clinical Internship

Education

Certified Data Analyst - Data Analysis

Doctor of Pharmacy - Pharm. D

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Scientific publication

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Drug Safety Associate

Clinical Internship

Certified Data Analyst - Data Analysis

Doctor of Pharmacy - Pharm. D

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