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Clinical research project manager with extensive pharmaceutical laboratory experience. Proven ability to communicate effectively and manage multiple tasks with meticulous attention to detail. Highly organized collaborative problem solver with excellent written and oral communication skills.
Yale Cancer Center
View- Company phone:
- (203)432-4113
- Company email:
- brita.belli@yale.edu
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Project ManagerYale Cancer CenterCheshire, Ct, Us -
Project ManagerYale Cancer Center Jan 2016 - PresentNew HavenProject Manager- Clinical Research Support Lab• Ensure proper execution of research lab collections for >90 active oncology clinical trials.- Determine feasibility of research lab collections for melanoma, phase 1 and hematology trials.- Attend site initiation visits to clarify protocol and lab manual discrepancies and discuss sponsor expectations.- Meet with study monitors during on-site visits to answer questions and obtain additional training.- Extract information from protocols regarding eligibility criteria and drug administration schedules.- Create detailed visit-specific templates for the collection, processing and shipping of specimens. - Enter specimen data into Oncore and MediData Rave databases.- Monitor kit and supply inventory using Barcloud and order supplies as needed.- Maintain extensive excel spreadsheets to track protocol milestones and deadlines.- Explore creative processes to facilitate complex research collections.• Serve as administrative liaison between disease teams, sponsors and clinical laboratory- Educate research lab staff to prepare for initiation of new studies.- Participate in weekly meetings with disease teams to discuss issues, timelines and priorities of upcoming and ongoing clinical trials.- Attend weekly regulatory meetings to discuss trial amendments and protocol deviations.- Document research lab protocol deviations and provide re-training as needed.- Provide timely and accurate data query resolution to both internal staff and external study coordinators.- Appointed to several specialty committees to research and propose improvements in workflows within the clinical trials organization.- Completed GCP, HRPP and HIPAA training.- SOCRA certified CCRP -
Research AssociateYale University School Of Medicine Oct 2012 - Dec 2015New Haven• Establish GI Oncology Biospecimen Repository- Consented >300 subjects to GI cancer biorepository.- Administered QoL and medical history questionnaires including semi-annual follow-ups.- Collected blood and surgical specimens and prepared RNA/DNA for sequence analysis.- Researched electronic medical records for relevant clinical data to supplement subject questionnaires.- Entered medical history, lifestyle data and biospecimen information into the Oncore clinical database to assess trends in treatment outcomes.- Created SOP manual to establish standardized operations for the newly established biorepository.- Determined research directions through literature reviews. -
Senior Research InvestigatorBristol-Myers Squibb Sep 1994 - Aug 2012Wallingford, CtExperience• Team leader for HIV high throughput screen using BSL-3 robotics system -Miniaturized whole-virus assay to 1536-well format -Optimized counterscreens for hit specificity (cytotoxicity, luciferase enzyme assay and MLV-based reporter systems)• Developed cell-based and biochemical assays for HIV and influenza programs -FACS and ELISA endpoints for compound/target competition assays to characterize leads -PAGE assays for protein oligomerization and endonuclease cleavage analysis for compound mechanism of action studies -High-content imaging for localization of viral proteins -Established reporter cell lines expressing cell surface receptors to evaluate novel co-receptor usage of HIV clinical isolates -Developed SPA-RT protocol to increase efficiency of anti-viral assay endpoints• Isolation of HIV and influenza clinical virus samples -Optimized protocol for amplifying HIV clinical isolates in primary T cells -PCR amplified influenza genes for cell-based assays and genotypic analyses• Pre-clinical evaluation of HIV inhibitors -Evaluated compounds for efficacy, cytotoxicity and human serum effects -Drug combination studies -Phenotypic and genotypic and characterization of resistance development• Prepared written reports and oral presentations for the scientific community• BSL-3 lab manager responsible for maintaining seamless daily operation of this specialized facility and ensuring the safety of personnel -
Post-Doctoral FellowFred Hutchinson Cancer Research Center Oct 1990 - Aug 1994Post-doctoral fellowConducted basic research to increase understanding of HIV biology -Established novel recombination assay to create chimeric viruses and evaluate the roles retroviral structural proteins play in virus assembly-Mentored graduate students from University of Washington-Contributed three 1st author publications to leading scientific journals and presented results at scientific meetings
Carol Deminie Skills
Carol Deminie Education Details
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Cell/Cellular And Molecular Biology -
Biochemistry
Frequently Asked Questions about Carol Deminie
What company does Carol Deminie work for?
Carol Deminie works for Yale Cancer Center
What is Carol Deminie's role at the current company?
Carol Deminie's current role is Project Manager.
What is Carol Deminie's email address?
Carol Deminie's email address is ca****@****ale.edu
What is Carol Deminie's direct phone number?
Carol Deminie's direct phone number is +120378*****
What schools did Carol Deminie attend?
Carol Deminie attended University Of Massachusetts Amherst, University Of New Hampshire.
What skills is Carol Deminie known for?
Carol Deminie has skills like Assay Development, Drug Discovery, High Throughput Screening, Virology, Elisa, Molecular Biology, Microsoft Excel, Clinical Research, Genomics, Mammalian Cell Culture, Immunocytochemistry, Cancer Research.
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