Lalitha Priya Chandrashekhar

Founder & CEO at PFG MedComm
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Contact Information
Location
New York City Metropolitan Area
Languages
  • English Native or bilingual proficiency
  • French Limited working proficiency
  • Telugu Native or bilingual proficiency
  • Hindi Limited working proficiency
  • Tamil Elementary proficiency

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LinkedIn User

Lalitha Priya is a detail oriented professional. She has a great technical knowledge and exceptional communication skills. I have worked with her on the LIMS implementaion project at Genzyme. She was a integral member of our team. I would highly revommend her.

Marléna McMahon-Purk, MSci

Priya is an absolute pleasure to work with--she is flexible, hard-working, and genuine. She'll take on the toughest deadlines and biggest jobs with a smile and energy that permeates the rest of the team. Her ability to adapt quickly, work well with team members, and her solid knowledge of science make Priya an asset to any workplace.

Roseann Kovelman

Priya is one of the most detailed and thorough writers I have ever worked with. She knew exactly what content the review committee would accept, what backup and references were needed, and how to prioritize jobs. Most importantly, our clients were always thrilled with the quality of work she produced. Her management skills, both with projects and people, are impeccable. She would be the first person I would call if I was ever in need of a writer and I sincerely hope we have the opportunity to work together again in the future.

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Credentials

  • Rationing and Allocating Scarce Medical Resources
    Coursera Verified Certificates
    Jul, 2013
    - Sep, 2024
  • Epidemiology & Biostatistics
    D&D Medical Writing Training
  • Regulatory Writing & Clinical Trial Reporting
    D&D Medical Writing Training

Experience

    • United States
    • Business Consulting and Services
    • 1 - 100 Employee
    • Founder & CEO
      • May 2014 - Present

      Accomplishing access through value communication. That's what we do. PFG MedComm is a strategic market access consultancy that is a certified woman- and minority-owned and led organization that specializes in leveraging value communication to achieve access goals. We’ve transformed the traditional agency model, our unique approach takes a holistic 360° view that considers the entire development lifecycle when planning for market access. Our proprietary process involves anticipating challenges, adapting strategic plans, and accomplishing access through seamless execution combined with wraparound engagement. As a full-service strategic market access agency, our capabilities run the gamut from the earliest stages of clinical planning and strategy through launch, training, and beyond. We are experts in developing end-to-end marketing strategies and tactics across all healthcare stakeholders, ranging from various types of payers (governmental, commercial, employer) and HEOR to healthcare professionals and patients. Our team has a broad range of experience in supporting medical, payer, and HEOR communication strategy across pharmaceutical, biotech, medical device, and digital therapeutic companies. Over the past ten years, the PFG MedComm team has supported over 60+ brands (including 33 launches both US and global) across 50+ indications within 20+ therapeutic categories. Let's talk about what we can accomplish together. Show less

    • Principal
      • Jan 2023 - Present

      PFG Stealth is a strategic consultancy for startups across the healthcare ecosystem (health tech, biotech, wellness, and medical). Capabilities: Go-to-market strategy, market access, launch planning, health economics and outcomes (HEOR), product development, value communication and value proposition development PFG Stealth is a strategic consultancy for startups across the healthcare ecosystem (health tech, biotech, wellness, and medical). Capabilities: Go-to-market strategy, market access, launch planning, health economics and outcomes (HEOR), product development, value communication and value proposition development

    • United Kingdom
    • Business Consulting and Services
    • 1 - 100 Employee
    • Mentor/Advisor
      • Aug 2022 - Present
    • United States
    • Research Services
    • 700 & Above Employee
    • Senior Manager, Value Communications, Global Health Economics and Outcomes Research
      • 2013 - 2014

      As a team lead within the Value Communications groups, provide guidance on strategic scientific communications and publication plans; develop a variety of scientific communications materials including manuscripts, congress abstracts/posters, health authority communications, clinical study reports, and slide decks. As a team lead within the Value Communications groups, provide guidance on strategic scientific communications and publication plans; develop a variety of scientific communications materials including manuscripts, congress abstracts/posters, health authority communications, clinical study reports, and slide decks.

    • United States
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Medical Communications
      • 2012 - 2013
    • Egypt
    • Human Resources
    • 1 - 100 Employee
    • Principal Medical Writer
      • 2011 - 2013

      Provide independent freelance medical writing and editing services for pharma projects for various clients including pharmaceutical ad agencies and life sciences firms. Provide independent freelance medical writing and editing services for pharma projects for various clients including pharmaceutical ad agencies and life sciences firms.

    • United States
    • Advertising Services
    • 1 - 100 Employee
    • Senior Medical Writer - Managed Markets, Payer, HEOR
      • 2011 - 2012
    • United Kingdom
    • Business Consulting and Services
    • 300 - 400 Employee
    • Scientific Communications/QC
      • Sep 2010 - Feb 2011
    • 1 - 100 Employee
    • LES Methods Expert Consultant
      • Aug 2009 - Sep 2010

      As a scientific Methods Expert, identified key requirements to ensure complete accuracy and compliance of ELN procedures using StarLIMS. As a scientific Methods Expert, identified key requirements to ensure complete accuracy and compliance of ELN procedures using StarLIMS.

    • United States
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Scientific App Specialist Consultant
      • Jun 2007 - Jun 2009

      As a Scientific Application Specialist, led the development of Velquest procedures for use in analytical, clinical and preclinical labs at Bristol Myers-Squibb. Worked with scientists, lab managers, and analysts from analytical, clinical and preclinical laboratories at three different BMS sites (US and UK) to define parameters and effective workflow for lab procedures specific to each department. As a Scientific Application Specialist, led the development of Velquest procedures for use in analytical, clinical and preclinical labs at Bristol Myers-Squibb. Worked with scientists, lab managers, and analysts from analytical, clinical and preclinical laboratories at three different BMS sites (US and UK) to define parameters and effective workflow for lab procedures specific to each department.

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Information Analyst Scientist Consultant
      • Jan 2007 - Apr 2007

      As an Information Analyst Scientist, developed chemical monographs for publication in the 15th edition of The Merck Index to reflect current scientific, medical and technological uses of compounds for most effective home or medical use. As an Information Analyst Scientist, developed chemical monographs for publication in the 15th edition of The Merck Index to reflect current scientific, medical and technological uses of compounds for most effective home or medical use.

    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Medical Regulatory Affairs
      • Jun 2005 - Aug 2006

      As the Regulatory Review consult, provided final review and approval of all information in major product websites, and related product collateral. Worked with Promotional Review Committee to review and approve various promotional and marketing materials prior to launch. Performed regulatory review of new websites at proposal stage and in test environment prior to launch, and responsible for regulatory review and audit of existing website content. As the Regulatory Review consult, provided final review and approval of all information in major product websites, and related product collateral. Worked with Promotional Review Committee to review and approve various promotional and marketing materials prior to launch. Performed regulatory review of new websites at proposal stage and in test environment prior to launch, and responsible for regulatory review and audit of existing website content.

    • United States
    • Pharmaceutical Manufacturing
    • QA Microbiology Lab Tech Writer
      • 2005 - 2005

      Authored a technical report submitted to internal and federal departments for review and implementation in the Microbiology Quality Control Lab. Authored a technical report submitted to internal and federal departments for review and implementation in the Microbiology Quality Control Lab.

    • Switzerland
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Oncology Biology Intern
      • Jun 2003 - Sep 2003

      As a summer intern in Oncology Biology, conducted research to analyze levels of HDAC expression as an indicative factor of cancer development. Project 1 : HDAC expression profiling in pre-cancerous and cancerous tissues Project 2 : Processing and analysis of clinical trial samples As a summer intern in Oncology Biology, conducted research to analyze levels of HDAC expression as an indicative factor of cancer development. Project 1 : HDAC expression profiling in pre-cancerous and cancerous tissues Project 2 : Processing and analysis of clinical trial samples

Education

  • Massachusetts Institute of Technology
    MIT-HMS Healthcare Innovation Bootcamp
    2021 - 2021
  • Drexel University
    Bachelor of Science, Biology, Psychology
    2002 - 2006

Community

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