Akbar Siddiq
Pharmacovigilance & Regulatory Writing Professional | Patient Safety Strategy, Risk Management, HA Interactions | DSUR • PBRER • RMP • Signal Detection
- Role
- Scientific Writer at 百时美施贵宝
- Location
- Hyderabad, TG, IN
- LinkedIn followers
- 500 followers
About Akbar Siddiq
In regulatory writing, Quality and Clarity isn\'t just a requirement, it\'s a responsibility. I am a seasoned pharmacovigilance and regulatory writing professional with a proven ability to communicate complex medical information clearly and accurately across multiple formats to support effective regulatory decision-making. I have a strong background in regional safety strategy, regulatory submissions, and benefit–risk management within the pharmaceutical industry. Expertise in regulatory documentation and signal detection support, including systematic scientific literature surveillance and end-to-end development of safety deliverables such as DSURs, PBRERs, PADERs, Risk Management Plans, and Implementation Effectiveness Plans, ensuring compliance with global and local regulatory requirements.Highly effective in Health Authority interactions and HA query responses, with strong cross-functional collaboration to drive aligned regulatory compliance and local risk management strategies (including KSA and Kuwait), across diverse therapeutic areas—consistently delivering high-quality, compliant pharmacovigilance documentation.Holds a Master’s degree in Pharmacology, with working knowledge of clinical research, product development, and global regulatory frameworks. Recognized for scientific rigor, strategic planning, operational excellence, and a strong commitment to patient safety.
Experience
Scientific Writer
Nov 2023 — Present · Hyderabad, IN
Education
Narayana junior college
Intermediate, (Bi. P.C.)
2005 — 2007
Osmania University
Bachelor of Pharmacy (BPharm)
2007 — 2011
Stanford University
Certificate Course, Writing in the Sciences
Jawaharlal Nehru Technological University
Master of Pharmacy, Pharmacology
2011 — 2013
Skills
- Medical Writing
- Pharmaceutics
- Drug Discovery
- Clinical Trials
- Molecular Biology
- Biochemistry
- Meddra
- Clinical Safety Narrative Writing
- Biotechnology
- Clinical Research
- Clinical Pharmacology
- Pharmacovigilance
- Gmp
- Hplc
- Clinical Safety Report (Csr)
- Clinical Operations
- Drug Delivery
- Pharmacokinetics
- Pharmaceutical Research
- Oncology
- Regulatory Affairs
- Lifesciences
- Pharmacology
- Cell Culture
- Pharmaceutical Industry
- Sop
- Glp
- Clinical Evaluation Report (Cer)
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