Open to opportunities

Talari Sreenivasulu

@talarisreenivasulu

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Clinical Research Specialist driving quality and operational excellence in trials.

India

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What I'm looking for

I am seeking clinical operations roles where I can apply RBQM, centralized monitoring, and eClinical tools to improve trial quality while growing into larger study leadership responsibilities.

I am a Clinical Research Specialist with four years' hands-on experience managing multi-country Phase II and Phase III clinical trials, focused on centralized monitoring, remote site management, and regulatory compliance.

At IQVIA I manage study operations with minimal supervision, driving risk-based monitoring, eTMF/ICF oversight, and data-driven insights to improve trial quality; previously I performed site initiation, monitoring, and regulatory submissions as a CRA and Clinical Trial Coordinator.

I have been recognized with company awards for proactive contributions and operational insights, and I hold an Advanced PG Diploma in Clinical Research & Pharmacovigilance plus Good Clinical Practice certification — I bring disciplined processes and collaborative stakeholder communication to deliver successful study outcomes.

Experience

Work history, roles, and key accomplishments

Current

Associate Centralized Monitor

Current

IQVIA

Feb 2024 - Present (2 years)

Managed multi-country Phase II/III studies with centralized monitoring, driving site performance improvements through QTL/KRI oversight and data-driven trend analysis; supported site lifecycle from activation to close-out. Recognized with Ovation Award (2024) for proactive insights to clients.

RBQM CTMS SAE AE Review Clinical Operations

Clinical Research Associate - I

Litemed India Pvt Ltd

May 2022 - Jul 2023 (1 year 2 months)

Coordinated and monitored clinical studies, conducted site qualification/initiation/monitoring visits, and managed regulatory submissions and eTMF documentation, contributing to timely study progress and compliance. Awarded Employee of the Year (2022).

Monitoring Regulatory Submissions ETMF IP Accountability

Clinical Trial Coordinator

Biofi Health Care India Pvt Ltd

Aug 2021 - Apr 2022 (8 months)

Supported protocol and document development, assisted ICF consent and enrollment processes, and ensured timely submission of safety reports and study updates to ethics committees and sponsors. Managed CRF/source documentation and investigational product accountability.

Safety Reporting Protocols Site Support IP Accountability

Education

Degrees, certifications, and relevant coursework

Santhiram College of Pharmacy

Doctor of Pharmacy, Pharmacy

Grade: 75%

Activities and societies: Research project on efficacy, safety, and cost effectiveness of generic and brand medications; published case reports in pharmacy/medical journals.

Completed Doctor of Pharmacy with a final GPA of 75% and conducted a comparative study on generic vs brand medications in diabetic patients; contributed case report publications.