Summary
Overview
Work History
Education
Skills
Languages
Personal Information
Research
Disclaimer
Certification
Timeline
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Eswari Subramaniyan

Eswari Subramaniyan

Chennai

Summary

A Pharm.D.(Doctor of Pharmacy)graduate, with an experience in a tertiary care multispecialty Hospital. Trained with good knowledge on ADR monitoring and reporting, patient care, counseling, vaccine safety basics and prescription monitoring. Interested in Healthcare AI, Precision Medicine, Pharmacometrics, Pharmacokinetics, Medicinal Chemistry, Research, Regulatory Affairs, Pharmacovigilance and Entrepreneurship. To be a part of and grow in an innovative organization that will provide me with a demanding and interesting environment, as well as opportunities for personal and organizational development. To share my academic knowledge and talents, as well as to work with the utmost passion and commitment.

Overview

2026
2026
years of professional experience
1
1
Certification

Work History

Author and Writer

  • Experience in writing news and publishing various scientific articles for promoting health care related information and published monthly newsletters
  • Performing activities and contributing ideas for research work
  • Access to Clinical resource toolkits (Lexicomp, Uptodate and Medscape)
  • Experience in writing, editing and making posters on health care information
  • Conducting activities and managing the team
  • Clinical drug calculations, interaction identifiers, overdose assessment, determine (PKPD) Pharmacokinetic-Pharmacynamic analysis to relate drug effect analysis training using PUMA Software
  • Formulary Development of a tertiary care hospital aims Indication, MOA, Dose and administration, Adverse effects and specific dosage adjustments for pediatric, geriatric and pregnancy/Lactation Population

Peer QC analyst - Senior safety aggregate report analyst

Pfizer pvt ltd
10.2023 - Current
  • Conducts and manages Aggregate Safety Report QC activities (PADER, PSUR, DSUR etc) produced by the Aggregate Report Center of Excellence (CoE) to ensure accuracy, internal consistency, uniformity and compliance with global aggregate reporting commitments
  • Serve as a Peer QC Subject Matter Expert (SME) on training, knowledge sharing, technology, or specific work processes, providing advice and guidance as appropriate
  • Collection of peer QC metric data for analysis
  • Support regulatory inspections, internal audits and/or strategic quality initiatives and familiarity with case processing (ICSR) and aggregate reports like PADER / PSUR
  • Demonstrated computer literacy, particularly in the use and management of relational databases
  • Demonstrated strength in analytical skills and attention to detail and project management tools

Clinical Pharmacist & Pharmacovigilance trainee / Research scholar

Sri Ramakrishna Multi Speciality Hospital
11.2022 - 12.2023
  • Prescription verification, validation, confirmation, reconfirmation and digitalisation
  • Handle the call to orders regarding Rx & Medicines
  • Flag the invalid prescription, arrange physician consultation
  • Patient Counseling regarding medications and supplements
  • Identifying Individual Case Safety Reports, Suspected adverse reactions (SAE) and Spontaneous reporting performed with technical product complaints and forwarding them to the relevant stakeholders within predetermined timelines
  • Handled and performed a systematic reporting of ADRs through Vigiflow database
  • Maintaining a library of responses to Frequently Asked Questions and of Standard Response Letters Perform through vigilance Screening
  • Participate as an active member of multidisciplinary teams to successfully achieve project goals
  • Identifying project issues and developing proposals for alternative strategies for discussion with superiors
  • Respond to unsolicited medical inquiries from healthcare professionals, patients/consumers, field staff and other internal business partners, regarding marketed products, investigation compounds, clinical trials and other product information
  • Process individual Case Safety Reports (ICSRs), including data entry in the electronic database
  • Entering information for medical information enquirers into medical information databases, tracking systems and project specific forms ensuring accurate data-entry
  • Check medications by reviewing and interpreting physician orders; detecting therapeutic incompatibilities
  • Control medications by monitoring drug therapies; advising interventions
  • Monitoring, documenting and reporting ADEs and ADRs
  • To verify all treatment sheets written by RMOs and consultants for appropriateness as per standards and report non-compliance on daily basis
  • Attend ward rounds with physicians checking the treatment plans and validation
  • To perform, list of audits on narcotic drugs, high alert medication, prescription and present the analysis as per calendar
  • Provides pharmacological information by answering questions and requests of health care professionals; counseling patients on drug therapy and disease management; lifestyle modifications
  • Documenting serious AEDs and ADRs and reporting following publication of the work and handling of clinical trial management systems
  • Quality Control Audit- 100 medication errors, 500+ prescriptions audited and reported
  • Actively participated in Infection control committee aid in research project and antimicrobial stewardship committee and emphasized on approval process of IRB/IEC
  • Maintains site payment and metrics
  • Conducts research protocol according to the Standard operating procedure(SOP), ICH guidelines and exponential knowledge on regulatory requirements of US -FDA/EMA
  • In depth knowledge about scientific medical terms and rare disease conditions
  • Alleviating disease conditions of various departments of General medicine includes Diabetology, nephrology, neurology, oncology, orthopedics, Pediatrics and Gynecology
  • Promote and comply with the ethics of hospital and maintain cordial relationship with the healthcare professionals adopt and plan effective treatment module for the patients specifically focusing on Precision medicine it's effects on the quality of life of the patient
  • Live demo sessions on eTMF Veeva Vault demo sessions and Microsoft sharepoint list tools to create a flow and perform other fundamental activities like review, scanning and indexing, quality control, copying, filing, forwarding or return to client/study teams and archiving
  • Preparation of essential documents: Informed consent, Documentation of CRF corrections, Investigator Brochure, Subject information sheet( SIS ) Clinical Documents, Investigational products accountability at the site, Recruitment advertisement and Amendments and managing Financial aspects of the trial
  • Project management and Indexing of documents with correct attributes and technical ( QC ) Quality Control analysis using the method of ALCOAA(Attributable, legible, contemporaneous, original, Accurate -complete)

Clinical research coordinator

Chennai Adyar cancer institute
03.2023 - 10.2023
  • A Phase 3 randomized controlled trial
  • Assessing the impact of omitting steroid (dexamethasone) and reducing the dose olanzapine in reducing vomiting and nausea in patients receiving chemotherapy
  • Conduct screening and counseling processes for potential study participants
  • Ensuring a comprehensive informed consent procedure is followed during participant enrollment
  • Managing the admission procedure, overseeing the smooth entry of participants into the study
  • Providing chemo counseling support to participants involved in chemotherapy interventions
  • Conducting study visits and implementing assessment procedures to monitor participant progress
  • Responsible for the assessment of toxicities and monitoring the overall quality of life (QOL) throughout the study duration
  • Daily patient follow-up

Education

PGDM Healthcare Management - Business Administration And Management

Welingkar Institute of Management
Mumbai (Hybrid)

Post Graduate Diploma In Strategic Marketing - Marketing Management And Research

Great Lakes Institute of Management
Chennai

Doctor of Pharmacy (Pharm.D) -

Sri Ramakrishna Institute of Paramedical Sciences
Coimbatore
01.2023

Higher Secondary Education -

Sakthi Vinayakar HinduVidyalaya
Thoothukud
01.2017

Secondary School Education -

Sakthi Vinayakar HinduVidyalaya
Thoothukudi
01.2015

Skills

  • MS Office
  • Adobe Photoshop
  • MS Outlook
  • Interpersonal skills
  • Soft skills
  • Statistical softwares
  • Public speaking
  • Healthcare AI
  • GMP
  • Clinical research
  • Psychology
  • Pharmacovigilance
  • Medicinal chemistry
  • Regulatory Affairs
  • Digital Marketing
  • Article writing
  • Accounting
  • Machine learning
  • Copywriting
  • Project management
  • Social services
  • Statistics
  • Organizational skills
  • Planning skills
  • Analytical skills
  • Problem-solving
  • Management
  • Leadership
  • Learning and adaptability abilities
  • MS Office
  • Scientific communication
  • Medical expertise
  • Medical writing
  • Therapeutic area proficiency
  • Healthcare industry awareness
  • Attention to detail
  • Problem-solving abilities
  • Patient safety
  • Adaptability and flexibility
  • Verbal and written communication
  • Decision-making
  • Effective communication
  • Risk management

Languages

English
Upper intermediate (B2)
Tamil
Advanced (C1)
Hindi
Intermediate (B1)

Personal Information

  • Date of Birth: 09/06/99
  • Gender: Female
  • Nationality: Indian
  • Marital Status: Single

Research

  • Evaluation of Restricted Antimicrobial Utilization in a Tertiary Care Hospital, 5, 6, 11/01/23, https://doi.org/10.36948/ijfmr.2023.v05i06.8834
  • Paraganglioma of Urinary Bladder - A case report, 09/01/21
  • A case report on Ewing's sarcoma with tumour excision, 09/01/21
  • A Case Report on Gliptins induced Bullous Pemphigoid, 11/01/23

Disclaimer

I hereby sincerely declare that all of the above-mentioned information is true or accurate to the best of my knowledge, and that I am solely responsible for the above-mentioned details.

Certification

Registered pharmacist certificate from Tamilnadu pharmacy council.

Timeline

Peer QC analyst - Senior safety aggregate report analyst

Pfizer pvt ltd
10.2023 - Current

Clinical research coordinator

Chennai Adyar cancer institute
03.2023 - 10.2023

Clinical Pharmacist & Pharmacovigilance trainee / Research scholar

Sri Ramakrishna Multi Speciality Hospital
11.2022 - 12.2023

Doctor of Pharmacy (Pharm.D) -

Sri Ramakrishna Institute of Paramedical Sciences

Higher Secondary Education -

Sakthi Vinayakar HinduVidyalaya

Secondary School Education -

Sakthi Vinayakar HinduVidyalaya

Author and Writer

PGDM Healthcare Management - Business Administration And Management

Welingkar Institute of Management

Post Graduate Diploma In Strategic Marketing - Marketing Management And Research

Great Lakes Institute of Management

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