Chirag Arora
⚕️ Safety Medical Writer ⚕️| Apcer Life Sciences | | M.Pharm in Pharmacology | | Researcher in Hepatotoxicity || Animal Research Specialist |
- Role
- Safety Medical Writer at Apcer Life Sciences
- Location
- Hisar, HR, IN
- LinkedIn followers
- 500 followers
About Chirag Arora
As an M.Pharm graduate in Pharmacology and former Assistant Professor at Om Sterling Global University, I have developed a strong academic and research background in pharmacological sciences, drug safety, and regulatory affairs. My postgraduate research focused on hepatotoxicity models, where I explored the protective role of Fumaric Acid in LPS and D-galactosamine induced liver injury in mice—contributing valuable insights into experimental pharmacology and therapeutic interventions.In my academic tenure, I mentored pharmacy students, coordinated examinations, and participated in curriculum development, honing my analytical, communication, and leadership skills. This experience helped me bridge the gap between theoretical knowledge and real-world applications in healthcare and research.Currently, I am working at Apcer Life Sciences as a Safety Medical Writer, specializing in aggregate reporting. In this role, I contribute to the preparation of Periodic Safety Update Reports (PSURs), Development Safety Update Reports (DSURs), and Risk Management Plans (RMPs), supporting global pharmacovigilance compliance and post-marketing surveillance efforts.I am passionate about ensuring drug safety and patient well-being through clear, evidence-based scientific communication. With a career grounded in research and a commitment to continuous learning, I aim to advance in the pharmacovigilance and regulatory writing landscape and contribute meaningfully to global healthcare systems.
Experience
Safety Medical Writer
Apr 2025 — Present · IN
Safety Medical Writing involves the preparation of scientifically accurate and regulatory-compliant documents that support drug safety and pharmacovigilance activities. As a Safety Medical Writer at Apcer Life Sciences, I contribute to the development of aggregate safety reports such as PSURs, DSURs, and RMPs. My work ensures timely and high-quality documentation for regulatory submissions, supporting the ongoing evaluation of benefit-risk profiles of medicinal products.
Education
College of Pharmacy, Pt. B.D.Sharma, PGIMS, Rohtak
B. Pharm, Pharmaceutical Sciences
I. K. Gujral Punjab Technical University (IKGPTU)
M. Pharm, Pharmacology
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