4+ years of qualitative experience in the healthcare industry. Areas of expertise include Clinical research, Oncology, Medical data analysis, Cytogenetics and Microbiology.
•Analysed and interpreted data from more than 20,000 medical and non-medical documents adhering to the guidelines using analytics tools.
•Salesforce handling for raising ticket to the client.
Clinical trial protocol and data
Analysed and interpreted data from more than 20,000 medical and non-medical documents adhering to the guidelines.
Handled Salesforce for raising tickets to the client.
Monitored clinical trials.
Performed company screening for drug research.
Screened publications and conferences for data extraction.
Created drug and trial database.
Screened trial and drug alerts.
Conducted clinical trial visits including site selection, CRA monitoring, patient screening, and follow-up visits.
Prepared clinical trial study documentation including subject recruitment, regulatory documents, ICF, CTA, IU, EC documentation, site feasibility form, TMF, ISF, study protocol amendments, and EC notification.
Maintained study logs including subject identification log, subject screening and enrolment log, subject visit log, IP temperature log, IP accountability log, IP retrieval log, delegation log, site training log, CRF transmittal log, protocol deviation log, and subject travel reimbursement log.
Worked on Phase 4 Dr. Reddys Transtuzumab study on patients with HER 2 +ve Cancer and Phase 4 Imbruvica study on patients with Chronic Lymphocytic Leukemia.
Performed karyotyping.
Performed Giemsa staining.
Cultured blood, bone marrow, and abortus samples.
Prepared slides.
Performed scanning.
Prepared reports.
Handled patient records and consent forms.
نظام التوظيف التشغيلي المعتمد على الذكاء الاصطناعي أولاً، الذي يوحّد ويؤتمت دورة التوظيف بالكامل للمؤسسات الحديثة حول العالم.
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