Summary
Overview
Work History
Education
Skills
Certification
Timeline
Generic
PRATIKSHA SINGRU

PRATIKSHA SINGRU

Philadelphia,PA

Summary

Motivated Medicine and Biomedical Science graduate with a strong passion for clinical research, medical writing, patient safety, and quality improvement. Equipped with robust analytical skills and a solid foundation in medical knowledge, expertise includes trial documentation, IRB preparation, data collection, and regulatory compliance, alongside conducting comprehensive literature reviews. Committed to simplifying complex scientific concepts to enhance accessibility of medical knowledge for diverse audiences. Actively seeking opportunities to contribute to innovative scientific endeavors and impactful medical education initiatives.

Overview

2
2
years of professional experience
3
3
Certification

Work History

Technical Writer (QC)

Cmic Cmo Usa
01.2025 - 06.2025
  • Prepared Certificates of Analysis (COA) developed Standard Operating Procedures (SOPs), Test Methods and managed documentation to ensure regulatory compliance and quality assurance.
  • Implemented feedback from end-users to continuously improve the quality and effectiveness of documentation materials.
  • Conducted regular reviews of existing documentation to keep it up-to-date and relevant.
  • Edited and proofread technical documents for accuracy and consistency.
  • Ensured all documentation complied with industry standards and legal requirements.
  • Summarized drug safety and lab findings into digestible reports for regulatory and cross-functional teams.
  • Maintained consistency across company documents by adhering to established style guidelines and templates.

Research Associate

Nous Bioscience (Startup)
09.2024 - 12.2025
  • Developed proficiency in modern cell culture techniques, including the maintenance, manipulation, and differentiation of various cancer cell lines.
  • Created technical reports and internal documentation summarizing findings from biochemical experiments and cell culture studies in oncology.
  • Assisted in experimental design to study molecular pathways, contributing to the understanding of cellular mechanisms.
  • Conducted comprehensive literature reviews to inform study designs and methodology decisions.
  • Gathered and organized information for research purposes.
  • Analyzed results using analytical software and created reports.
  • Participated in lab meetings and project presentations.

Assistant Grant Writer

Virufy
03.2024 - 09.2024
  • Drafted competitive grant applications and research proposals for projects focused on AI-based diagnostics for COPD.
  • Wrote and organized IRB protocols, consent forms, and regulatory documents aligned with funding agency requirements (NIH, private foundations).
  • Conducted comprehensive literature reviews to support scientific rationale and background for grant submissions.
  • Developed structured case report forms (CRFs) and data collection tools to support compliant clinical study execution.
  • Assisted in developing impactful grant applications to enhance organization's potential for funding awards.
  • Organized material to research and complete writing tasks.
  • Edited and proofread technical documents for accuracy and consistency.

Research Assistant

Jefferson Health
10.2023 - 03.2024
  • Reviewed imaging findings in collaboration with radiologists and translated them into concise research reports and summaries.
  • Created slide decks and scientific presentations for departmental meetings and research dissemination.
  • Conducted literature reviews to support data interpretation and contextualize research findings.
  • Collaborated closely with clinical research coordinators, physicians, and fellows to manage datasets, ensure HIPAA compliance, and prepare materials for internal review and presentations.
  • Participated actively in regular meetings with fellow researchers to discuss project updates, challenges faced, and lessons learned during ongoing activities.
  • Conducted literature reviews to support hypothesis development and identify gaps in existing knowledge.

Clinical Documentation Specialist

IKS Health Pvt. Ltd
09.2022 - 05.2023
  • Created patient visit summaries from physician dictations using EPIC EMR, contributing to case narratives for clinical records.
  • Ensured consistency and compliance in clinical documentation based on regulatory standards and clinical guidelines.
  • Reviewed and edited medical notes to ensure accuracy, clarity, and readability for healthcare professionals.

Education

Master of Science - Biomedical Sciences

Drexel University
Philadelphia, PA
09.2025

M.D. -

Texila American University College of Medicine
Georegetown, Guyana
04.2022

Skills

  • Scientific & Medical Writing
  • MS office
  • Literature Review & Analysis
  • Clinical Research Documentation
  • Regulatory Writing (SOPs, Protocols, COAs)
  • IRB Submissions & Ethical Compliance
  • Manuscript Preparation
  • Grant Writing
  • Data Interpretation & Summarization
  • Medical Terminology & Clinical Guidelines
  • Evidence-based Writing
  • Technical Writing
  • GCP, ICH, FDA Guidelines
  • AMA Style
  • ICMJE Criteria

Certification

  • Medical Writing Skills for Beginners, The Good Clinical Practice (GCP)
  • Project Management: Healthcare Projects, Statistics Foundations 1: The Basics
  • Patient Privacy and Confidentiality, Writing in Science

Timeline

Technical Writer (QC)

Cmic Cmo Usa
01.2025 - 06.2025

Research Associate

Nous Bioscience (Startup)
09.2024 - 12.2025

Assistant Grant Writer

Virufy
03.2024 - 09.2024

Research Assistant

Jefferson Health
10.2023 - 03.2024

Clinical Documentation Specialist

IKS Health Pvt. Ltd
09.2022 - 05.2023

Master of Science - Biomedical Sciences

Drexel University

M.D. -

Texila American University College of Medicine

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