Kulpreet KAUR

Experience

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  Santosh University, Ghaziabad

  Sept 2014 - Sept 2015

  General Dentist (Co-Op)

  Clinical Expertise Working proficiently in clinical set-up, highly coordinated and collaborative and upgraded with latest equipment in the field.Root Canal TreatmentsWell conversant with RC procedures and associated treatment, had worked on multiple RC cases with complications and verity.Prosthesis and Tool ExtractionsDecent exposure of prosthesis and various level of tool extraction procedures and worked on multiple cases with expertise and precisionImpaction and Tool ScalingWell experienced in general dental clinical processes like dental scaling and impactions. Show less

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  Dental Life Hospital

  Sept 2015 - Feb 2019

  General Dentist

  Examined patients’ medical records Prepared patients for treatment (e.g. by applying oral sedation or anesthesia) Checked teeth, gums, and other parts of the mouth, along with X-rays and tests, to diagnose dentalproblems Worked on cleaning, Plaque removal, and cavity fillings, dental prosthetics [bridges, crowns, anddentures etc.] Conducted tooth extractions and root canal procedures with limited to no supervision Performed surgeries on diseased tissues and bones

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  Sarvin Sabet Psychological Services

  Mar 2019 - Aug 2021

  Clinical Administrative Manager

   Accessed the patient file- add all patient information and insurance information in Universal Booked new referrals, pre-screens, assessments, treatment, etc. Took all incoming calls, and enquires from lawyers, and psychologists for non-compliance with treatments, insurers, etc. designate inquiries to the appropriate department to follow through with responding to inquiries. Created OCF-18s for psych assessments and psych treatments, obtained signatures, and submittedthem to insurers. - printed hard copy to file. Compiled and shared all medical documents of clients including assessment reports, pre- screening, progress report, session notes, and log sheets when requested by referral resource upon confirmation of release by the Clinical Coordinator. Obtained monthly Excel spreadsheet of service dates for patients from the psychologists andprocessed payments. Cross-referenced SOAP notes and excel dates for payments of psychologists. Tracked all the completed sessions, assessments, and pre-screenings by the providers and updatedthe dates on Universal Show less

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  Cliantha Research Limited

  Sept 2021 - now

  Clinical Research Coordinator

   Co-leading early and late phase clinical trials encompassing all the administrative duties and supervisionof clinical operations under the direct oversight of the Principle Investigator. Leading clinic operations for studies and co-ordinating study-related tasks in complete accordance withthe protocol requirements. Administrative handling of studies including the creation of all source documents as per protocolrequirements, creating regulatory binders, and training of staff on the same. Ensuring study start-up regulatory compliance including NOL from Health Canada. Delivering informed consent to research volunteers/subjects in a common way of communicating everysingle aspect of the study, investigational product, and more importantly their rights. Handling volunteer database i.e. Alphadas to keep their information updated for all common users andeffective management. Recording any treatment-emergent or pre-treatment Adverse Events and their handling until resolutionincluding their reporting to the IRB, sponsor / Health Canada within the time as required. Recording and tracking any deviations relating to Protocol / SOP / GDP / PIOP etc. further to haveinvestigator's impact assessment, QA evaluation and further closing after corrective and preventiveactions and re-trainings. Also for major/critical deviations involving subject safety, initiating promptescalation to the sponsor and IRB / Health Canada. Protecting subject/volunteer’s personal information in accordance with federal and provincialregulations such as PIPEDA and PHIPA respectively. Finalization of eCRF in coordination with the data management team to reflect paper CRF and othersource documents as per protocol. Leading trial closeout procedures including but not limited to data management, soft lock, hard lock,trial close audit, and site close-out visits under strong liaison with the project manager. Show less