Experience

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  It bhu

  Jun 1997 - Jun 2001

  B.pharm student
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  Smithkline beecham

  Jan 2000 - Jan 2000

  B.pharm trainee

  Learnt about GMP manufacturing of different formulation like tablets, capsules, injections, ointment and syrups

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  Bits pillani

  Jan 2001 - Jan 2003

  Me biotech student
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  Niper

  Jan 2001 - Jan 2002

  Jrf

  Worked on Novel Drug Delivery system. Prepared clotrimazole loaded vaginal film for vaginal infection

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  Itrc

  Jan 2003 - Jan 2004

  Trainee
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  Pgimer chandigarh

  Sept 2003 - Jun 2004

  Research scholar

  Worked as a research Scholar on a project entitled as "Targeted Delivery of Tuberculosis Drug"

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  Nii - national institute of immunology

  Jul 2005 - Apr 2012

  I was involved with curcummin nano particle formulation for the targeted delivery for GIT/colon cancer. I worked as a PhD student at National Institute of Immunology, Delhi. I have been awarded PhD in November 2011.My PhD project was entitled as "Immuno-genicity and Protective efficacy of Dry powder inhale-able formulation of Mycobacterium W". My area of interest is development of Novel Delivery system for Drugs and vaccineTargeted Delivery for cancer therapyImmunology of Infectious diseases.

  • Post Doctorate Fellow

    Nov 2011 - Apr 2012

  • Senior Research fellow

    Jul 2005 - Nov 2011
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  Institute of nuclear medicine and allied science (defence research and development organization

  May 2012 - Jun 2014

  Research associate at inmas (drdo)

  Product Development and Delivery: Led the development of innovative medical solutions, including the "Chitosan Wound Sealant," "Indigenous Pain Assessment Tool," 4 mg Melatonin Nasal Drop for brain radioprotection, 10 mg Nalbuphine Hydrochloride Sublingual Injections for acute pain in emergency warfare, and 5 mg Nalbuphine Base Nasal Drop for efficient analgesic delivery. Successfully delivered 350 units of the Chitosan Wound Sealant to CRPF, contributing to critical medical support.• Research Conduct and Reporting: Conducted extensive research on various pharmaceutical products, overseeing formulation optimization, efficacy evaluation, and safety assessment. Prepared comprehensive reports documenting research findings and methodologies, ensuring transparency and knowledge dissemination.• Mentorship and Guidance: Provided mentorship and guidance to PhD scholars and research trainees within the department, fostering a collaborative and supportive research environment while nurturing talent for future scientific endeavors.• Interdepartmental Collaboration: Collaborated with other departments and research teams within DRDO INMAS to leverage expertise and resources, driving interdisciplinary research initiatives and facilitating the development of new and innovative medical products.• Nanoparticle-based Inhalation System Development: Currently working on the development of a nanoparticle-based inhalation system for radio-pharmaceuticals, aiming to enhance drug delivery efficiency and therapeutic efficacy.• Clinical Trial Participation: Engaged in Phase II clinical trials of various inhalation and oral formulations of decontamination agents, contributing to the evaluation of their safety and efficacy for potential deployment in critical scenarios. Show less

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  Icgeb, delhi

  Jan 2014 - Jul 2015

  Senior research associate

  1. Experimental Planning: Collaborating with the research team to design and plan new experiments aimed at optimizing the preparation of nanoparticles with maximum peptide loading, ensuring efficient drug delivery to the brain.2. Execution of Experiments: Overseeing the execution of both cell-based and animal-based experiments to evaluate the efficacy of the peptide nanoparticles. This involved meticulous attention to detail and adherence to experimental protocols to generate robust and reliable data.3. Cell-Based Studies: Conducting cell culture experiments to assess the uptake and biological activity of the peptide nanoparticles in relevant cell models of Alzheimer's disease, providing valuable insights into their potential therapeutic efficacy.4. Animal Studies: Designing and conducting animal studies to evaluate the in vivo efficacy and safety of the peptide nanoparticles, including assessments of brain penetration, therapeutic effects, and potential adverse effects.5. Data Analysis: Analyzing experimental data to derive meaningful conclusions regarding the performance of the peptide nanoparticles, contributing to the overall project objectives and informing further research directions.6. Collaboration: Collaborating with international partners and stakeholders involved in the project, including researchers, clinicians, and industry collaborators, to facilitate knowledge exchange and drive progress towards the development of novel therapeutics. Show less

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  Indian spinal injury centre, delhi

  Mar 2017 - May 2024

  Head, basic research

  As the Head of the Research Department, my Key Result Areas (KRAs) encompass a comprehensive range of responsibilities aimed at driving research excellence and fostering impactful collaborations.1. Leadership and Management: Providing dynamic leadership and effective management to the Research Department, ensuring alignment with organizational objectives and fostering a culture of innovation and excellence.2. Strategic Planning and Budgeting: Developing and implementing strategic plans for the Research Department, including comprehensive budget planning and resource allocation to support research initiatives effectively.3. Project Management: Overseeing the successful execution of all sponsored trials and academic clinical trials to the highest standards, ensuring adherence to timelines, quality standards, and regulatory requirements. Successful completed Phase I/IIa academic trial for the treatment of pressure ulcers in individuals with SCI. Additionally, lead post-marketing study on knee implants as the lead for Site Management Organization (SMO). 4. Ethics Committee Management: Serving as the Member Secretary for ISIC's ethics committees, overseeing ethical review processes for research projects, and ensuring compliance with ethical guidelines and regulations.5 Data Presentation and Review: Presenting project data for internal (Scientific Advisory Board meetings) and external scientific review processes, demonstrating transparency, and facilitating constructive feedback.6. Project Development and Grant Writing: Spearheading the development of new research projects, writing research grants, and securing funding to support innovative research endeavors that address critical healthcare challenges. 7. Stakeholder Engagement: Engaging with funders, academicians, government representatives, policymakers, associates, and supporters to build strong collaborations, solicit support, and enhance the impact of research outcomes.. Show less

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  Indian spinal injury center new delhi

  Dec 2019 - May 2024

  Head basic research laboratory and administrator bone bank at india spinal injury center

  I established Bone Bank and Pharmacovigilance department at ISIC and hence given addition charge of Administrator Bone Bank and Head of Pharmacovigilance. I've spearheaded a range of critical responsibilities to ensure the seamless operation of our bone donation and pharmacovigilance processes. My key duties include:• Evaluation and Approval: Thoroughly evaluating documentation for both donors and recipients, and approving suitable donors for bone donation. Facilitating the donor consent process with meticulous attention to detail.• Storage and Sterilization: Ensuring proper storage and sterilization procedures are followed meticulously post-donation to maintain the integrity of donated bone tissue.• Regulatory Compliance: Compiling monthly and annual reports for submission to government authorities, and conducting audits to ensure compliance with regulatory standards.• Stakeholder Coordination: Liaising closely with doctors to guarantee comprehensive documentation for bone recipients, fostering a seamless process from donation to transplantation.As the Head of Pharmacovigilance:• Training and Oversight: Conducting training sessions for all stakeholders to enhance awareness and adherence to pharmacovigilance protocols.• Adverse Reaction Reporting: Ensuring accurate and timely reporting of all adverse reactions, maintaining strict compliance with regulatory requirements.• External Collaboration: Collaborating with PvPI (Pharmacovigilance Programme of India) for reporting on their portal, fostering transparency and accountability.• Protocol Adherence: Overseeing PvPI coordinators to ensure all activities align with established protocols, guaranteeing robust pharmacovigilance practices. Show less