RESUME
KEERTHI G
OBJECTIVE:
Aspiring clinical research professional with a solid academic foundation in microbiology and
biotechnology, complemented by pharmaceutical industry experience and a strong life science
background. Possessing a keen interest in Clinical Research, Clinical Data Management,
Regulatory Affairs, and Pharmacovigilance. Seeking an entry-level role in clinical research or
healthcare data management to apply my scientific expertise, pharmaceutical knowledge, and
regulatory understanding in ensuring data integrity, patient safety, and compliance with
industry standards. Eager to contribute to innovative research and regulatory processes in a
dynamic healthcare environment.
EDUCATION:
YEAR OF PASSING INSTITUTION
M Sc
[Microbial Technology]
2024 REVA University, Bengaluru.
B Sc
[Chemistry, Botany, Zoology]
2021 MES College of Arts, Commerce and
Science, Bengaluru.
12th
[PCMB]
2018 Soundarya PU College, Bengaluru.
10th 2016 Srushti Public School, Bengaluru.
PROJECT WORK:
Clinical Microbiology: A Comparative study of different sample types to detect clinically significant
hemoglobin variants using mass spectrometry. [Anand Diagnostic Laboratory, Queens Road, Bengaluru].
SKILL DEVELOPMENT PROGRAMME:
• Processing, value addition and quality Assessment of Millets.
[University of Agricultural Sciences [GKVK], Bengaluru]
• Fundamentals on Medical Biochemistry and Pharmaceutical Microbiology. [DR Biosciences,
GangaNagar, Bengaluru]
TRAINING PROGRAMME:
Hands-on Training on “Downstream processing technology” [Biozeen, Bengaluru]
EXPERIENCE:
Worked as IP QA [Quality assurance] in liquid manufacturing unit,
for 6 months at Recipharm Pharma Services, Bengaluru.
CERTIFICATION:
• Completed 6 Months Certification on Clinical Research, Clinical Data Management Regulatory
Affairs and Pharmacovigilance from Guardians Ed Tech (2023 – 2024).
• Good Clinical Practice (GCP) Certificate of completion from the NIDA Clinical Trials Network
(2024).
INTERESTED AREAS:
• Clinical trials, Clinical data management, Pharmacovigilance, Medical Writing,
Regulatory affairs, clinical research associate, clinical research coordinator, Drug safety
associate.
SKILLS:
• Good knowledge about Good Clinical Practice (GCP) Guidelines, Good manufacturing
practice (GMP).
• Good theoretical knowledge of pre-Clinical study and clinical trial (All four phases).
• Good understanding of adverse event, serious adverse event, side effect, drug abuse, drug
misuse, drug overdose, drug underdose etc.
• Theoretical knowledge of Pharmacovigilance.
• Familiar with the regulatory authorities. ([hidden], FDA, ICH-GCP, EU Guidelines) Ethical
Considerations in Human Subjects Research.
• Knowledge of statistical analysis and data validation processes.
• Strong attention to detail, excellent communication skills, and team collaboration.
• Proficient in Microsoft Excel, Microsoft PowerPoint, Microsoft Word.
PERSONAL DETAILS:
Father: GANGANNA KR
Mother: NAGARATHNA R
DOB: 02/07/2000
Gender: Male
Nationality: Indian
Marital Status: Single
Languages: Kannada, English, Hindi.
PERMANENT ADDRESS:
#01, SAMRUDDHI NILAYA, HEGGADADEVANAPURA, ALUR ROAD, NEAR MAKALI,
DASANPURA HOBLI, BENGALURU NORTH, BENGALURU 562162.
KEYWORDS:
Clinical Research, Clinical Data Management, Regulatory Affairs, Pharmacovigilance, Medical Writing, Good Clinical Practice, Good Manufacturing Practice, FDA, ICH-GCP.
“`
Cover Letter:
Keerthi G
Bengaluru, India
13 February 2025
Hiring Manager
Medgenome
Bengaluru
Subject: Application for Genome analyst Position.
Dear Hiring Manager,
I am excited to apply for the genome analyst position at Medgenome. With an [hidden] in Microbial Technology and certification in Clinical Research, I bring expertise in clinical trials, data management, and regulatory compliance. My experience in quality assurance at Recipharm Pharma Services and hands-on training in microbiological techniques equip me to contribute effectively to your team.
I look forward to the opportunity to discuss how my skills align with your needs. Thank you for your time and consideration.
Sincerely,
Keerthi G
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