Chandrapaul Parsram

Experience

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  Walgreens

  Aug 2015 - Aug 2017

  Certified Pharmacy Technician

  -Communication: Clearly and concisely communicate orally and in-print to patients, pharmacists, and providers to resolve insurance rejections, concerns about drug interactions, and questions regarding medical history-Detail-Oriented: Verify legitimacy of written scripts by ensuring State Board standards; Process written scripts into database for insurance adjudication; Fill medications while maintaining high quality and accuracy to ensure public safety and patient privacy-Interprofessional Competency: Collaborate with healthcare professionals to assist patients with medication management to improve medication compliance and adherence Show less

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  Be The Match

  Sept 2017 - Feb 2018

  Biorepository Intern

  -Industry Comprehension: Provide support and work on projects in multiple areas including: registry repository, consent form processing, on-line registration, research repository, and kit-making business unit to better understand the operations involved in the management of the Bone Marrow Registry-Health Advocacy: Contribute towards the overall goal of growing the bone marrow donor registry to increase the likelihood of patient-donor match; Participate in outreach to recruit donors with diverse background to advocate for patients that are underserved by the registry. -GDP and PHI Experience: Experience using Good Documentation Practices on documents to manage workload and trace specimens in the repository; Processing forms with Protected Health Information to determine donor eligibility Show less

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  Pace Analytical

  Jun 2018 - Sept 2019

  Regulatory Affairs Coordinator

  -Coordinate and process certificate submissions to support OUS device registration for 3M Unitek and ESPE products; Assist product associate with Post-Marketing Surveillance Reports to support Clinical Evaluation Reports and ISO standards compliance to support Audit preparation-Conduct label assessment to assist with update for compliance with EU MDR compliance for class I and II medical devices-Create, manage and maintain Hazard Communication documents including Safety Data Sheets and labels for new and existing internal materials and commercial products-Contact 3M raw material vendor for EHS&R inquiries including regulated lists, RoHS/WEEE, REACH/SVHC, global inventories, local, state, federal and global regulations-Work with manufacturing sites to obtain formulation, composition and regulatory information Show less

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  3M

  Sept 2019 - Apr 2024

  -Manage regulatory inputs for devices in Abrasives and Infection Prevention portfolio of 3M ESPE Dental Products- Assess and document the impact of product changes on medical device regulations in the US, EU, Brazil, Japan, and Australia -Create regulatory assessments of packaging artwork to identify gaps in EU MDR labeling requirements and outline changes for compliance -Support the EU MDR transition project by identifying gaps in the General Safety and Performance Requirements of legacy products and coordinate documents requirements with functional business groups Show less

  • Senior Regulatory Affairs Associate

    Nov 2022 - Apr 2024

  • Advanced Regulatory Affairs Associate

    May 2021 - Nov 2022

  • Regulatory Affairs Associate

    Sept 2019 - May 2021
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  Solventum

  Apr 2024 - now

  -Maintain support for activities required for marketed products, including license renewals, regulatory assessments for product changes, technical files and global registration dossier, as well as reviewing and approving documents such as Post-Market Surveillance Update Reports (PSURs), Clinical Evaluation Reports (CER), Clinical Development Plans (CDP), labeling, and claims-Develop and execute regulatory strategies for new product development programs in key markets such as the U.S., Brazil, Japan, Australia, Canada, China, and the E.U. Show less

  • Senior Regulatory Affairs Specialist

    Aug 2024 - now

  • Regulatory Affairs Specialist

    Apr 2024 - Jul 2024