Sohini Sengupta Email and Phone Number
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• Ability to lead and supervise interdisciplinary project teams, prioritize workloads, and deliver results. • Strong problem solving, analytical and organizational skills.• 10+ years of experience in successfully conducting research projects from their conception to completion. • Highly knowledgeable of clinical trial (Phase I-Phase III) and observational cohort study designs. • 2 years of work experience at an investigational clinical site for AIDS clinical trials, and 1 year of experience working on a multi-site clinical trial on eating disorders.• 10+ years of experience in monitoring and evaluation. Activities include protocol development and training for research team members; and ensuring accordance of standardized operating procedures (SOPs) related to data collection, data management, and data analysis.• Therapeutic and/or patient education expertise in the following diseases/conditions: HIV/AIDS, influenza, tuberculosis, eating disorders, depression, alcohol/substance use, domestic violence, cardiovascular disease, and arthritis.• 9 years of experience working in bioethical issues associated with human research protection; highly knowledgeable of U.S. regulatory requirements for protecting patient-subjects in clinical trials, including Good Clinical Practices (GCPs), Informed Consent Forms (ICFs), and other Institutional Review Board (IRB) requirements.• 15+ years of experience in scientific/technical writing and interpretation of the medical literature. • 10+ years of experience as external reviewer for scholarly medical and public health journals. • Proficient in Microsoft Office, SPSS, and Endote.Specialties: academic, brochure design, conferences, consulting, data analysis, data collection, data entry, data management, database administration, english, forms, grant writing, medical writing, meeting facilitation, mentoring, microsoft access, microsoft powerpoint, presentation skills, process engineering, progress, project management, protocols, recruiting, research, scientific writing, spanish, structured methods,
Unc-Chapel Hill
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Research Assistant ProfessorUnc-Chapel Hill Jun 2002 - Present• Principal Investigator on an NIH Career Developmental (K01) Award to study vulnerable populations in AIDS clinical trials.Project Managemento Developed and implemented three research projects: Project 1 studied AIDS clinical trial investigators’ perceptions of U.S. federal regulations on vulnerable populations in AIDS clinical trials; Project 2 studied the relationship between therapeutic misconceptions of AIDS clinical trial enrollees and their motivations to participate in AIDS clinical trials; Project 3 tested the effectiveness of an educational intervention to improve informed consent understanding among newly enrolled AIDS clinical trial participants. o Developed standardized protocols, data collection forms, and codebooks to collect and manage data.o Hired, trained, and supervised research assistants in patient/investigator recruitment, data collection, and data analysis.Monitoring and Evaluationo Developed tracking system to assess response/refusal rates, monitor loss-to-follow-up, collect data at follow-up time points. o Validated data entry for database management, and cleaning data for data analysis.o Developed and submitted IRB protocols (including consent forms in English and Spanish) and progress reports to the UNC-Chapel Hill Biomedical IRB and GCRC. Wrote and submitted an adverse event report to the IRB for one project.o Established DSMB for Project 3, and developed and presented interim and final reports to the DSMB.Scientific Writingo Wrote NIH KO1 grant which was awarded funding for five years.o Wrote manuscripts as primary author for Projects 1-3; Project 1’s manuscript is under review in a scholarly journal, and Projects 2-3 are under review by other co-authors and soon will be submitted.o Abstracts were accepted and posters presented at the 13th Conference of Retroviruses and Opportunistic Infections and the International AIDS Conference in Toronto, Canada. PowerPoint was used to create the posters. -
Research AssociateUnc-Chapel Hill Apr 2001 - Jun 2002• Co-Investigator on Duke Endowment grant to evaluate access and utilization of hospice and end-of-life care services in North Carolina. Project Management, Evaluation, and Monitoring, Scientific Writingo Co-wrote and awarded Duke Endowment. o Recruited hospice service organizations.o Developed protocols, data collection forms, and codebooks to collect and manage data to measure access and utilization.o Developed tracking system to assess response/refusal rates of service organization contacts.o Validated data entry for database management, and cleaning data for data analysis.o Analyzed data.o Developed and submitted IRB protocol (including consent forms) and progress reports to the UNC-Chapel Hill Biomedical IRB.o Co-wrote manuscript of findings that was published in scholarly journal• Project Coordinator for subcontract with Duke University to understanding the structure and processes of Institutional Review Boards (IRBs) that oversee clinical research.Project Management, Evaluation, and Monitoring, Scientific Writingo Reviewed documents of IRBs’ standard operating procedures and manuals.o Developed and administered a standard interviewing examining IRBs’ training, protocol review, and structure. o Analyzed data collected from document reviews and interviews.o Wrote and submitted report to a national Clinical Research Oversight Committee.• Scientific Writing Coordinatoro Developed and disseminated brochures to educate pregnant women about HIV testing in prenatal care in English and Spanish.o Provided education, consultation, and mentoring to UNC faculty, Fellows, and students the development of their own NIH and private foundation grants that focused on vulnerable populations, end-of-life-care, or other bioethics issues.
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Postdoctoral FellowUcsf Jul 1999 - Apr 2001• Co-Investigator on NIH RO3 grant to explore pregnant women’s perceptions of routine HIV testing in prenatal care in three different U.S. sites.• Project Lead Coordinator of study to explore perceptions of community and non-academic members on IRBs nationwide. For both projects:Project Management, Evaluation and Monitoring, Scientific Writingo Developed and implemented standardized protocol to recruit and interview patients/participants.o Developed codebooks for data management and analysis.o Hired, trained, and supervised research assistants in data management and analysis.o Developed tracking system to assess response/refusal rates of patients/participant at each site.o Developed and submitted IRB protocols (including consent forms in English and Spanish) and progress reports to UNC and other institutions’ IRBs.o Managed and analyzed data. o Wrote manuscripts of findings that were published in scholarly journals.• Research Associate on a Health Research and Services Administration (HRSA)-funded case study to examine disparities in access and utilization of antiretroviral drugs in three states.Project Assistance, Evaluation and Monitoring, Scientific Writingo Assisted with the development and conduct of structured interviews of health officials and providers.o Assisted with data management and data analysis.o Co-wrote manuscript of findings that was published in scholarly journal.• Other Scientific Writingo Converted doctoral dissertation to manuscript that was published in scholarly journalo Co-wrote NIH RO3 grant. -
Research CoordinatorStanford University Medical Center Jul 1994 - Aug 1995Central Research Coordinator for three industry-sponsored multi-center clinical trials assessing the effects of cognitive behavioral therapy, Prozac, or the combination of both in reducing the symptoms or characteristics of anorexia and/or bulimia.Project Management, Evaluation and MonitoringDeveloped standardized operating procedures (SOPs) and other study documents (e.g., questionnaires).Train other sites' study coordinators to use SOPs.Recruited patient-subjects for three studies. Prepared site-visit reports and organized site-visits. Worked with Principal Investigator on evaluation/monitoring strategies, including developing a tracking system to monitor data collection time points, and loss to follow-up; regular communication with other site coordinators to monitor protocol implementation and track any problems; develop timelines.Prepared Powerpoint presentations for Principal Investigator to present at meetings. -
Clinical Research AssistantAids Clinical Trials Group Jul 1989 - Jun 1991Research Assistant to the Principal Investigators for the ACTG at the Stanford site. Project Management, Evaluation and Monitoring, Scientific WritingDeveloped and Implemented protocols of in vitro sub-studies that used blood specimens of clinical trial subjects. Studies focused on the detection and quantification of human immunodeficiency virus RNA in patient serum by use of polymerase chain reaction, and checking for antiretroviral effects on plasma viremia. Developed standard operating procedures and tracking system for collecting and storing blood specimens; train internal staff to use SOPs.Administered standardized questionnaires to clinical trial patient-subjects.Prepared slide presentations for investigator meetings and conferences.Prepared site-visit reports.Co-wrote manuscripts for both in vitro projects that were published in scholarly journals.
Sohini Sengupta Skills
Sohini Sengupta Education Details
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Biological Sciences
Frequently Asked Questions about Sohini Sengupta
What company does Sohini Sengupta work for?
Sohini Sengupta works for Unc-Chapel Hill
What is Sohini Sengupta's role at the current company?
Sohini Sengupta's current role is Research Assistant Professor at UNC-Chapel Hill.
What is Sohini Sengupta's email address?
Sohini Sengupta's email address is se****@****med.unc
What schools did Sohini Sengupta attend?
Sohini Sengupta attended University Of North Carolina At Chapel Hill, San José State University, San José State University.
What skills is Sohini Sengupta known for?
Sohini Sengupta has skills like Research, Education.
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Sohini Sengupta
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Sohini Sengupta
Director Of Research Development Under The Office Of The Vice Provost For ResearchChapel Hill, Nc4unc.edu, unc.edu, duke.edu, duke.edu1 +191996XXXXX
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