Indranath Paramanik

About Indranath Paramanik

I am a results-driven Registered Pharmacist with nine years of experience in Pharmacovigilance and five years in Pharmaceutical Marketing. My expertise spans end-to-end pharmacovigilance operations, including ICSR review & submission, PV compliance, SOP authoring, risk management, and stakeholder engagement. I have successfully led global pharmacovigilance teams, ensuring adherence to international regulatory standards (FDA, EMA, MHRA, NMPA) while driving process excellence and operational efficiencies. Most recently, at DDReg Pharma Pvt. Ltd, Gurugram, I managed a team of 10-12 professionals handling 20+ drug portfolios across the US and UK markets. My focus has always been on optimizing processes, ensuring compliance, and delivering high-quality safety data analysis to support risk-benefit assessments and enhance drug safety. With a Post Graduate Diploma in Business Administration (Marketing Management) and a Bachelor’s in Pharmacy, I complement my pharmaceutical expertise with strong business acumen. Additionally, my certifications in: Lean Six Sigma (Yellow, Green, Black, Master Black Belt) – Driving process improvements, operational excellence, and efficiency. Certified Scrum Master – Agile project management, cross-functional team collaboration, and continuous improvement. I am passionate about leveraging my analytical skills, leadership abilities, and compliance expertise to strengthen pharmacovigilance frameworks and enhance patient safety. Let’s connect! Reach me at i••••••••@gmail.com to explore opportunities in Pharmacovigilance, Compliance, and Operational Excellence.

Experience

1. Assistant Manager

   DDReg Pharma Pvt. Ltd.

   Dec 2022 — Present · Gurugram, IN

   I supervise a team of 8 -10 members in managing end-to-end pharmacovigilance processes for approximately 20 drugs from clients in the USA and UK, including those regulated by the FDA, MHRA, and NMPA.As Assistant Manager, I lead my team to achieve both individual and collective goals, providing training to enhance their skills in safety monitoring and case processing. I conduct regular performance reviews, offering feedback and setting developmental goals.I oversee case processing to ensure accuracy and compliance with SOPs, making sure serious adverse events are reported on time. I prioritize tasks and monitor submissions to the USFDA and MHRA, while ensuring quality checks on processed cases.Furthermore, collaboration is key in my role. I liaise with Clinical, Medical Affairs, and Regulatory Affairs teams to integrate safety data and manage relationships with CROs and vendors for effective case processing. I also work closely with IT to maintain safety databases.Strategically, I identify areas for process improvement and lead initiatives to optimize workflows. I stay updated on global pharmacovigilance regulations and oversee budget management to support my team. In times of crisis, I guide my team through unexpected safety issues with marketed products.Lastly, I ensure all documents are archived appropriately and maintain pharmacovigilance databases. I prepare billing data, generate project reports, and analyze adverse event data to identify trends and emerging risks.

Education

• Gupta College of Technological Science, Asansol, West Bengal, India (Affiliated by WBUT & PCI)

  Bachelor of Pharmaceutical Technology

  2006 — 2010

• Symbiosis Centre for distance Learning (SCDL), Pune, India

  Post Graduate Diploma in Business Administration (PGDBA)

  2011 — 2013

Skills

• Sales & Marketing
• Business Development
• Pharmaceutical Sales
• Market Analysis
• Market Research
• Presentation and Training
• Client Management
• Quality Assurance
• Market Planning
• Sales Promotion
• Budgeting
• Direct Sales
• Team Management
• Marketing Strategy
• Product Management
• Pharma Product Sales
• Marketing Solutions
• Business Development & Strategy
• Sales Planning & Execution
• Technical Presentations
• Competitor Analysis
• Market Intelligence
• Client Interaction
• New Product Launch
• New Markets Development
• Brand Management
• Publicity & Promotions
• Customer Relationship Management (Crm)
• Liaison & Coordination
• Strong Interpersonal Skill
• Pharmacovigilance
• Data Analysis
• Clinical Data Management
• Meddra
• Clinical Trial Management System (Ctms)