---
title: "Shreyas Sadekar - Senior Performance Lead - Office of the CMO in Bengaluru | Tal"
description: "Meet Shreyas Sadekar, IIM Bangalore | GSK | Project Management, Change Management, Strategic Communications Ex-Novo Nordisk, Ex-Springer Nature based in Bengaluru. AI stack includes claude code, gemini, and grok."
image: "https://tal.club/meet/shreyas-sadekar/share-image"
---

# Shreyas Sadekar on Tal

## Headline

IIM Bangalore \| GSK \| Project Management, Change Management, Strategic Communications Ex\-Novo Nordisk, Ex\-Springer Nature

## About

Supporting crucial tech initiatives in GSK's Office of the Chief Medical Officer, my focus is on driving project and change management practices that enhance strategic communications and stakeholder relationships\. I am committed to excellence, evidenced by multiple recognitions for delivering high\-quality outcomes\. As part of the organization’s vision, I am dedicated to supporting clinical research advancements through effective management and clear, compliant communication, ultimately contributing to the betterment of patient care and therapeutic development\.

## Location

Bengaluru

## AI stack

claude code

gemini

grok

notebooklm

openai

claudecode

## Work experience

Senior Performance Lead \- Office of the CMO at GSK, Nov 2025 \- Present · 1 yr, Greater Bengaluru Area

Performance Lead \- Office of the Chief Medical Officer at GSK, Jan 2024 \- Nov 2025 · 1 yr 11 mos, Bengaluru, Karnataka, India, Project Management, Change Management, Strategic Communications, Tech initiatives Overview, Stakeholder Management

Manager \- Clinical Trial Transparency at GSK, Jun 2021 \- Dec 2023 · 2 yrs 7 mos, Bengaluru, Karnataka, India

Senior Medical Writer at Novo Nordisk, Nov 2017 \- Jun 2021 · 3 yrs 8 mos, Bengaluru, Karnataka, India, Currently working on writing non\-interventional study \(NIS\) reports in a complex programme of NISs, intended for effectiveness analysis of approved products in real\-world clinical practice\. Involves end\-to\-end involvement including associated project and stakeholder management\. Writing Investigator brochures \(IBs\)\. Subject matter expert \(SME\) for writing and reviewing layperson summaries of phase 1\-4 interventional clinical trials\. Posting clinical trial results on US \(ClinicalTrials\.gov\) and European \(EudraCT\) registries as per regulations\. Expertise in redaction of interventional and non\-interventional clinical trial documents including but not limited to CSRs, protocols and SAPs\. Project Management involving forecasting of annual workload\. Developing and updating existing templates associated with clinical trial disclosure deliverables\. Development and management of new processes around multiple aspects surrounding clinical trial disclosure activities

Scientific and Medical Writer \- Adis Insight at Crest \(part of the Springer Nature group\), Feb 2015 \- Nov 2017 · 2 yrs 10 mos, Pune Area, India, Reviewing and writing key results about the efficacy, safety and tolerability, and pharmacokinetics and pharmacodynamics of the drug from published clinical trial data and media releases\. Consolidating information after extensive literature search from multiple sources and creating accurate and concise summaries from various clinical trial registries\. Writing and updating clinical data of all the proprietary drugs in clinical phases\. Tracking the clinical progress of various drugs from the clinical to marketing stage\. Reviewing published clinical literature from leading medical journals, abstracts presented in conferences, media releases, and clinical trial registries\.

Medical Writer I at Cactus Communications, Aug 2014 \- Jan 2015 · 6 mos, Mumbai Area, India, Current responsibilities include compendia surveillance and summarizing recent updates for a multinational client

Medical Writer I at Sciformix, Mar 2013 \- Jul 2014 · 1 yr 5 mos, Pune Area, India, Core labeling activities – drafting new and amendment of existing source labels –USPI \(United States Package Insert\), SmPC \(Summary of Product Characteristics\), PIL \(Patient Information Leaflet\), Medication guides etc\. Conversion of labels into Health Authority prescribed formats – PLR and QRD conventions\. Meeting BOH labeling submission requirements and deadlines of submission\. Proficient with FDA and EMA labeling submission categories\. Preparation of Company core data sheets\. Coordinating with internal stakeholders/ SMEs for data contribution to labels\. Managing labeling teams and organizing LT meeting with SMEs based across the globe\. Coordinating labeling operations specialists and label QCers for effective management of labeling project\. Conversion of labels to SPL and other formats for HA submission\.

## Education

Executive General Management Program, Business Administration and Management, General, Indian Institute of Management Bangalore

M\. Pharm, Quality Assurance Techniques, Sinhgad College of Pharmacy

[View the original profile](https://tal.club/meet/shreyas-sadekar)

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