Praneeth Barra

About Praneeth Barra

With over 15 years of experience in the clinical research and pharmaceutical industries, I am a seasoned professional dedicated to driving success across the full lifecycle of clinical trials—from Phase 1 to Phase 4, including proof of concept and BA/BE studies. My expertise encompasses Clinical Data Management, Biostatistics, Statistical Programming (SDTM, ADaM, TLFs), Clinical Operations, and Clinical Monitoring, where I consistently deliver high-quality client outcomes for clients.I am passionate about ensuring the best quality deliverables for my clients and contributing to the success of their clinical pipelines and products. My experience also extends to Real-World Evidence projects, empowering clients to leverage data for informed decision-making.In the Medical Devices sector, I have extensive knowledge of Clinical Evaluation Reports (CER), Medical Device Regulation (MDR) compliance, and labeling requirements, including Instructions for Use (IFU) and electronic IFU (eIFU). Additionally, I support Drug Discovery and Chemical Development, helping clients navigate early-stage research challenges and advance their initiatives.As the Director & Head of Business Development, I focus on fostering strategic, long-lasting partnerships within the clinical research, pharmaceutical, biotechnology, and medical device industries. I thrive in environments that require a blend of scientific insight, technical expertise, and business acumen. By providing tailored solutions and high-value services, I aim to drive growth and success for my clients in today’s competitive landscape.

Experience

1. Director & Head of Business Development

   Invitro Research Solutions Private Limited

   Feb 2025 — Present

   is a Bangalore-based Contract Research Organization (CRO) offering end-to-end support across the drug development and clinical research lifecycle. We serve Pharmaceutical, Biopharmaceutical, Medical Device, and Nutraceutical companies with a focus on quality, compliance, and cost efficiency.At iVRS, we provide a comprehensive range of services including: Clinical Operations, Project Management, Site Management, and Monitoring : CDM strategy, EDC setup, data entry, validation, and database lock & : Statistical analysis, SDTM/ADaM datasets, and TLFs : Protocols, Investigator Brochures, CSR, and Regulatory Writing : Case processing, signal detection, and aggregate reporting : Extractables & Leachables (E&L), Nitrosamine studies, IVRT/IVPT, method development and validation : Dossier compilation, submission strategy, and global regulatory guidanceWith our strong scientific team, 21 CFR Part 11-compliant infrastructure, and proven track record in regulatory submissions (USFDA, EMA, Health Canada, and SFDA), we help clients accelerate timelines and reduce development costs by up to 30–40%.

Education

• Acharya Nagarjuna University

  Master of Technology (M.Tech.)

  2012 — 2014

• Sri Krishnadevaraya University

  Bachelor of Technology (B.Tech.)

  2008 — 2012