Evan Cimino Email & Phone Number

Wilmington, Delaware, United States

• Lead the daily operation of a small team of high performing scientists in support of drug discovery and development programs.
• Responsible for weekly ADME screening, mechanistic assays to address compound/program specific needs and preclinical compound characterization to support IND filings.
• Work with a wide variety of in vitro assays and further develop current technologies to enhance in vitro assays, including protein binding, clearance, Caco2 permeability, PAMPA… Show more
• Work with a wide variety of in vitro assays and further develop current technologies to enhance in vitro assays, including protein binding, clearance, Caco2 permeability, PAMPA, etc.
• Designed and implemented detailed protocols to train new team members on laboratory procedures and assays, improving onboarding efficiency and reducing training time while ensuring consistency and accuracy.
• Work closely with DMPK Principal Investigators and Directors on issue driven mechanistic ADME studies.

Wilmington, Delaware, United States

• Responsible for DMPK support of discovery and development projects including bioanalysis of PK and TK study samples
• Perform LC-MS/MS quantitation of samples in a regulated, GLP setting. Including:o Sample Analysiso Validationo Method development
• Independently analyze data, record data, prepare summary documents, and report data (written and oral) as needed
• Conducted regulated bioanalysis for multiple clinical trials across Phase 1 to Phase 3, ensuring compliance… Show more
• Conducted regulated bioanalysis for multiple clinical trials across Phase 1 to Phase 3, ensuring compliance with regulatory standards while managing concurrent programs to support drug development efforts
• Review study data as required

Wilmington, Delaware, United States

• Collaborated with clients to generate leads, identify growth opportunities, and enhance business development initiatives across laboratory and clinical research markets.
• Consulted and assisted in the development of sales and business development strategies, targeting pharma and CROs on behalf of clinical research sites to grow the sites’ pipeline with applicable trials.
• Supported multi-vendor laboratory instrumentation services, including maintenance, repair, installation, and… Show more
• Supported multi-vendor laboratory instrumentation services, including maintenance, repair, installation, and qualification for LC/MS, HPLC, ICPMS, and other advanced analytical platforms.
• Contributed to the development and customization of IQ, OQ, and PQ protocols to ensure compliance with laboratory standards and optimize instrument performance.
• Assisted in establishing preventative maintenance schedules to enhance instrument reliability and minimize downtime for diverse laboratory equipment. Show less

Newark, DE

• FDA, GLP/GCP-compliant contract research organization supporting discovery, preclinical and clinical drug development.
• Perform analysis of biological samples (plasma, urine, whole blood, serum, tumor and tissue) for the quantitation of proprietary and generic compounds and GLP methods.
• Proficiency in extracting compounds from test matrix using liquid-liquid separation, solid phase extraction and protein precipitation extraction techniques, including automation.
• Perform run… Show more
• Perform run set up on LC-MS/MS equipment using Analyst software.
• Operation of Tomtec Quatra 4 96-well automated sample extraction system.

Newark, DE

• Act as a liaison with clients and CROs regarding incoming and received biological samples, drug substances, and compounds.
• Use Watson LIMS for complex sample entry, study design, sample and analytical data tracking, and reconciliation.
• Act as technical resource, trainer, and troubleshooter for Sample Coordinators.
• Communicate directly with Supervisor and Management for operational and/or technical improvements.
• Responsible for handling and recording all samples sent to QPS… Show more
• Responsible for handling and recording all samples sent to QPS to insure compliance with FDA regulations, GLP’s, and QPS SOP’s and maintaining proper paperwork and approval. Show less

Newark, DE

Bachelor’S Degree, Biological Sciences

Activities and Societies: Anthropology Minor

Pre - Physician Assistant Coursework

Activities and Societies: Phi Theta Kappa Honors Society