Susan Tantawi, Dabt Email and Phone Number
Susan Tantawi, Dabt work email
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Susan Tantawi, Dabt personal email
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Susan Tantawi, Dabt is a Founder and Principal Toxicologist at Akcella Consulting Firm, Inc.. She possess expertise in cro, glp, clinical development, drug development, toxicology and 39 more skills. Colleagues describe her as "I had the pleasure to work with Susan for more than a year on various projects and various vendors. Susan supported us as a sponsor representative and study monitor for outsourced preclinical studies and related analytical tasks. I found her support really helpful in planning, placing, designing, monitoring and reporting of studies and study progress. She supported Molecular Partners a lot in identifying the best suitable vendor, time slot and price. She provided valuable input on a scientific as well as on a regulatory/formal level. Her response times are minimal and she stays on top of things even in busy times. She is very competent and customer-focused. I enjoyed very much working with her.", "I have had the pleasure of working with Susan for about 4 years now and I have always been impressed with her work ethics. Susan is a detail oriented, extremely organized, intelligent and very reliable Project Director. No matter how complex the project she is assigned, time and again she will deliver results impeccably.", and "We worked on a pre-clinical IND study. She was monitoring closely all aspects of the study. She also continuously updated CRL involved personnel of the program status. It was a pleasure to work with Susan."
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Founder And Principal ToxicologistAkcella Consulting Firm, Inc.Montreal, Qc, Ca -
Founder & Principal ToxicologistAkcella Consulting Firm, Inc. 2024 - PresentMontreal, Quebec, Ca -
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Vice President, Toxicology & Nonclinical DevelopmentGalecto, Inc. Jan 2023 - Dec 2023 -
Senior Director, Toxicology & Nonclinical DevelopmentGalecto, Inc. Jan 2021 - Jan 2023 -
Director, Toxicology & Nonclinical DevelopmentGalecto, Inc. Dec 2014 - Jan 2021 -
Manager Business DevelopmentCitoxlab North America Inc. Sep 2014 - Nov 2014Evreux Cedex, Fr -
Project DirectorInsymbiosis Jul 2011 - Aug 2014Designed and managed multiple regulatory toxicology projects and managed pre-clinical IND enabling programs. Was accountable for a pre-clinical project throughout its entirety - starting at the project planning phase, through the coordination of project execution up to data analysis and report writing. Performed all aspects of management of research projects including: - Initial discussions with clients (external and internal) through to writing of scientific plans, protocols and proposals - Budget creation and management - Project execution through management of research activities via outsourcing strategies - Solving of scientific and logistical problems - On-site monitoring of in-life activities at the CROs and writing of detailed monitoring reports for clients- Data analysis, report writing and presentation to clients - Accountable for the scientific quality of all projects as well as their delivery on time and on budget- Attendance of meetings and interactions with the regulatory authoritiesScientific Expert:- Provided scientific input and strategy into new as well as existing scientific programs- Scientific interface between the Company and its clients as well as between the Company’s scientific and commercial groups- Scientific champion in the area of regulatory toxicology and pre-clinical IND enabling studies
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Client Portfolio CoordinatorCharles River Laboratories Jun 2010 - Jun 2011Wilmington, Massachusetts, Us- Served as an advocate with the company for selected clients.- Was responsible for introducing key client-specific requirements and subsequently monitoring compliance to these requirements with feedback to senior scientific management.- Facilitated and resolved issues raised by the client or the staff internally. - Acted as an internal resource person for client specific details including development pipeline and therapeutic classes in development. -
Research Scientist Ii - Inhalation ToxicologyCharles River Laboratories Dec 2007 - Jun 2011Wilmington, Massachusetts, UsJob responsibilities included:- Complete oversight of toxicology studies ranging from acute to chronic in a GLP environment.- Experience in conducting inhalation studies with reproductive and safety pharmacology components including respiratory and cardiovascular endpoints.- Writing a complete study protocol based on the study design and required evaluations and endpoints.- Monitoring prestudy and in-life phases of the study and assure that all tasks performed by technicians are in compliance with the protocol and regulatory guidelines.- Interpretation of study data and writing a complete integrated report which is provided to the Sponsor for submission to the appropriate regulatory agencies.- Assisting Sponsors in designing preclinical toxicology studies that meet the regulatory requirements based on the class of compound and proposed use.- Working with the Business Development department and providing scientific assistance for new inquiries.- Validating new procedures and techniques.- Writing standard operating procedures. -
Technician - Inhalation ToxicologyCharles River Laboratories Jan 2006 - Dec 2007Wilmington, Massachusetts, Us- Performed in-life portion of inhalation toxicity studies.- Set-up the inhalation exposure laboratory for each study based on the study protocol and requirements. - Performed pre-study aerosol characterization including concentration and particle size distribution assessments.- Recorded all study data as per GLP regulations. -
Online Teacher - Computer ApplicationsConcordia University Sep 2004 - Jun 2007Montreal, Qc, Ca- Provided online assistance to students ranging from first to final year of undergraduate degree as well as continuing education students; group size ranged from 50-150 students per semester.- Graded students’ assignments and quizzes and provided feedback to individual students requiring improvement.- Maintained spreadsheet to track students’ overall performance for final course evaluation.- Invigilated on-site during final examinations. -
Teaching Assistant - Histology/Advanced HistologyConcordia University Sep 2004 - May 2005Montreal, Qc, Ca- Provided laboratory assistance for students enrolled in Histology and Advanced Histology courses.- Assisted course professor in preparing laboratory examinations and was responsible for grading and evaluating the students for the laboratory aspect of the course.- Prepared powerpoint presentations and guidances to assist students in preparing for laboratory examinations.
Susan Tantawi, Dabt Skills
Susan Tantawi, Dabt Education Details
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Concordia UniversitySpecialization Biology
Frequently Asked Questions about Susan Tantawi, Dabt
What company does Susan Tantawi, Dabt work for?
Susan Tantawi, Dabt works for Akcella Consulting Firm, Inc.
What is Susan Tantawi, Dabt's role at the current company?
Susan Tantawi, Dabt's current role is Founder and Principal Toxicologist.
What is Susan Tantawi, Dabt's email address?
Susan Tantawi, Dabt's email address is su****@****ail.com
What schools did Susan Tantawi, Dabt attend?
Susan Tantawi, Dabt attended Concordia University.
What skills is Susan Tantawi, Dabt known for?
Susan Tantawi, Dabt has skills like Cro, Glp, Clinical Development, Drug Development, Toxicology, Drug Discovery, Pharmaceutical Industry, Pharmacology, Oncology, Sop, Life Sciences, Project Management.
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