Naga Srilakshmi Jonnalagadda
Hyderabad
Summary
Highly motivated and skilled pharmacy graduate with a strong foundation in medical terminology, drug safety and clinical research. Possessing a Master of Pharmacy with a CGPA of 8.8, academic experience includes hands on work in analytical research and active participation in workshops and seminars related to clinical research and regulatory affairs. Technical expertise encompasses Drug safety regulations, safety data bases, clinical data management, electronic data capture and informed consent process. Strong communication, teamwork and problem solving skills are among key attributes, with a commitment to patient safety in an entry level drug safety and clinical research role.
Overview
1
1
Certification
Work History
Project Intern
Innovative Pharma Solutions
07.2022 - 09.2022
¢ Assisted in the Analytical research department of Biological formulations by following SOPs
¢ Actively participated in quality checks, ensuring adherence to regulatory standards.
¢ Communicating with superiors and colleagues regarding regulatory standards and research process.
- Balanced needs of as many as 2-3 projects at one time
Project Trainee
Aurobindo Pharma Research Center
04.2022 - 06.2022
- ¢ Assisted in Analytical research department of Topical formulation by following SOPs
- ¢ Actively participated in quality checks, ensuring adherence to regulatory standards.
- ¢ Successfully managed project time lines, reflecting strong time management skills and ability to meet guidelines.
- ¢ Collaborate with peers on academic projects, showcasing effective team work and commitment to project goals.
- ¢ Showcased strong problem skills by identifying and resolving issues promptly
Education
Master's - Pharmacy
KVSR Siddhartha College of Pharmaceutical Sciences
Vijayawada, AndhraPradesh12.2022
Bachelor's - Pharmacy
VIPW
Vijayawada, India10.2020
Intermediate - Biology
Sri Chaitanya Junior College
Vijayawada, Andhra Pradesh05.2016
SSC -
St Paul's Public School
Vijayawada, Andhra Pradesh05.2014
Skills
- MS office
- Basics of Regulatory requirements and guidelines
- Good clinical practices
- Familiarity with clinical research principles, clinical trials and research knowledge
- Adverse event reporting, serious adverse event handling
- Safety reporting process
- Clinical data management,
- Electronic data capture, Informed consent process
- Medical terminology, Human anatomy and Physiology
- Familiar with safety data bases and SAS coding
- Administrative support
- Team support
- Data Collection
Accomplishments
- Collaborated with team of 6 in the development of
Project on Novel RP-HPLC Method
Development and Validation for simultaneous estimation of clindamycin Phosphate and Methyl Paraben in topical gel formulations done in Aurobindo Parma Research Centre .
Certification
Clinical research and data management - ClinIndia
Pharmacovigilance and SAS coding - Clinlogics
Quality management principles of Medical devices - Alison
Timeline
Project Intern
Innovative Pharma Solutions
07.2022 - 09.2022
Project Trainee
Aurobindo Pharma Research Center
04.2022 - 06.2022
Master's - Pharmacy
KVSR Siddhartha College of Pharmaceutical Sciences
Bachelor's - Pharmacy
VIPW
Intermediate - Biology
Sri Chaitanya Junior College
SSC -
St Paul's Public School
Clinical research and data management - ClinIndia
Pharmacovigilance and SAS coding - Clinlogics
Quality management principles of Medical devices - Alison
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