Lopamudra

Create and proofread scientific content for electronic publication, journals, and infographics. Transcribe medical webinars or audio dictations into text and use that material to build accredited CME activities like online courses, slide decks, and interactive modules for healthcare professionals in accordance with the publication style guides. Screen literature (eg, PubMed, Ovid search, and Cochrane Library), medical terminology, clinical trial databases, and various evidence-based treatment guidelines.

Copy editor (Freelancer) at TNQ TECH PRIVATE LIMITED (2021-10 – 2026-07)

• Create and proofread scientific content for electronic publication, journals, and infographics.
• Transcribe medical webinars or audio dictations into text and use that material to build accredited CME activities like online courses, slide decks, and interactive modules for healthcare professionals in accordance with the publication style guides.
• Screen literature (eg, PubMed, Ovid search, and Cochrane Library), medical terminology, clinical trial databases, and various evidence-based treatment guidelines.

Associate Report Analyst (Home based) at Larvol (2016-09 – 2018-02)

• Responsible for conducting daily secondary search and deliver high-quality reports and insights to clients.
• Associated with KOL programs and performed analysis for research articles, publications, clinical trials, scientific or healthcare conferences in the healthcare industry.

Quality Assurance Manager Consultant at InnoVision Therapeutics Inc. (2010-06 – 2016-09)

• Responsible for quality assurance and regulatory compliance in the clinical development of the pharmaceutical products and nutraceuticals.
• Review of Clinical Trial Protocols, Investigators' Brochure, Informed Consent Documents etc.

Research Associate (Clinical QC) at GVK Bio Sciences Pvt Ltd (2007-09 – 2010-05)

• Lead the Internal Quality Team to ensure planning, coordination, control, and continuous improvement of processes and methods to control the quality of studies.
• Worked closely with clinical operations and other supporting areas, development teams, to help ensure active participation in continuous quality improvement activities.
• Train and supervise the team on trial-specific collection, review and approval of documents and associated processes.

Clinical Research Associate at PLIVA Research India Pvt Ltd (2006-04 – 2007-06)

• Prepared and reviewed study protocols, investigator brochure/SMPC, case record forms, informed consent forms, and subject information sheet, etc.
• Was responsible for monitoring the trial to ensure its compliance with established regulatory standards, such as Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and applicable regulatory requirements.

Certification in Global Regulatory Affairs – Biotecnika (2026-05 – 2026-08)

Masters in Clinical Research – Institute of Clinical Research (2006)

Bachelors in Pharmacy – Biju Patnaik University of Technology (2004)