Syed Rahil Azam
Bangalore,
Summary
I am a Pharm.D graduate with a strong foundation in clinical pharmacology, drug safety monitoring, and regulatory compliance. Demonstrated knowledge in adverse event reporting, signal detection, and risk management aligned with FDA, EMA, and ICH guidelines. Focused on applying strong research skills toward improving data management, organization and reporting. Strong analytical and communication skills with a passion for improving animal and human health outcomes though data-driven safety evaluation. Eager to contribute to innovation and responsible healthcare by ensuring the highest standards of drug safety and vigilance.
Overview
2
2
years of professional experience
2
2
years of post-secondary education
1
1
Certification
Work History
Intern
PES University Institute of Medical Sciences & Research
12.2024 - 11.2025
- Gained hands-on clinical exposure through direct involvement in patient care and medication management.
- Performed prescription auditing, identified medication errors, and ensured safe and effective drug therapy.
- Conducted drug interaction analysis and supported therapeutic drug monitoring to optimize patient outcomes.
- Collaborated with physicians, nurses, and healthcare teams to provide evidence-based treatment recommendations.
- Educated patients on medication usage, safety, and adherence.
Clinical Research Trainee
Apollo Hospital
Bengaluru
01.2024 - 08.2024
- Conducted a prospective observational study titled 'Comparative Evaluation of Adverse Reactions by Contrast Media – Non-Ionic Monomer vs Non-Ionic Dimer'.
- Collected, analysed, and documented patient data related to contrast-induced adverse drug reactions.
- Performed risk assessment and identified patterns of adverse reactions to improve patient safety.
- Collaborated with radiologists and clinical teams to ensure accurate data collection and adherence to GCP.
Education
Doctor of Pharmacy (Pharm.D) -
PES Institute of Pharmacy
Bengaluru 07.2018 - 01/2025
Higher Secondary Education (PCMB) -
Sri Vidya Mandir Hr. Sec. School
06.2016 - 04.2018
Skills
- Protocol design
- Case report forms
- Informed consent
- ADR reporting
- Signal detection
- Risk management
- Designing clinical studies
- Conducting clinical studies
- Analysing clinical studies
- Drug interactions
- Therapeutic drug monitoring
- Dosage optimization
Core Interests
- Clinical Research & Clinical Trials
- Clinical Data Management
- Pharmacovigilance & Drug Safety
- Research & Publications
- Clinical Pharmacology
- Machine Learning in Healthcare
Certification
- Drug Development and Product Management — Coursera.
- ICH-GCP Principles & Code of Federal Regulations (CFR) — NIH.
- Pharmacovigilance & ADR Modules — PvPI India.
- Master Clinical Research Comprehensive Basic Guide — Udemy.
Languages
English
Proficient
C2
Tamil
Proficient
C2
Hindi
Proficient
C2
Urdu
Proficient
C2
Kannada
Intermediate
B1
Training
- 2nd ID CONGRESS: Infectious diseases and antimicrobial stewardship in critical care congress - 2024.
- Workshop on Clinical Research: Clinical software – Hands-on training with Bangalore Clinical Research Institute (BCRI).
Publications
- Comparative Evaluation of Adverse Reactions by Contrast Media (Prospective Observational Study) – Clinical Radiology Journal (Under Review).
- Effect of Melatonin on Nocturnal Blood Pressure and Dipping Pattern in Non-Dipper Hypertensive Patients Receiving Standard Antihypertensive Therapy – Ongoing.
- A Rare Case Report of Oral Prednisolone-Induced Dementia — 2025.
Timeline
Intern
PES University Institute of Medical Sciences & Research
12.2024 - 11.2025
Clinical Research Trainee
Apollo Hospital
01.2024 - 08.2024
Doctor of Pharmacy (Pharm.D) -
PES Institute of Pharmacy
07.2018 - 01/2025
Higher Secondary Education (PCMB) -
Sri Vidya Mandir Hr. Sec. School
06.2016 - 04.2018