Emily Kitts Email & Phone Number

Morton, PA, US

Minato-ku, Tokyo, JP

• Assists with preparing, writing, editing, and finalizing analytical, clinical and/or documents as assigned, including but not limited to: analytical study procedures, protocols and reports; clinical study protocols and.
• Assists with the content of design control documents
• Assists in the development of templates, style guidelines, and SOPs.
• Edits documents; performs macro-editing of documents for organization, content, structure, and tone, and to ensure documents are consistent; performs micro-editing of documents for punctuation, grammar, sentences.
• Assists with scheduling the internal review of documents.
• Reviews for internal consistency of data, accuracy and completeness of references, etc. for technical, clinical, analytical and other regulatory documents including scientific abstracts.

Wilmington, Delaware, US

• Performed QC review, proofreading and accuracy checks of GLP pre-clinical and clinical study reports and NDA/IND submissions to FDA
• Edited SOPs; wrote and maintained work instructions to improve and streamline processes
• Led, managed and organized the process of archiving study-related physical and electronic documents for Bioanalysis and Toxicokinetics groups, including processing proper documentation in the EDMS, creating and.
• Developed specimen inventory disposal initiative which resulted in a cost savings of $130,000 per year
• Served as interim Sample Manager, which included accessioning sample and study data using LIMS, receiving biospecimens and pulling samples from inventory when requested by scientists in the department for assay work

Raleigh, North Carolina, US

• Provided daily support to project team members in clinical operations and project management
• Assisted with the management of patient recruitment vendors to increase study enrollment through advertising
• Developed and maintained study documents and utilized company systems to manage clinical/biomedical studies
• Tracked, dispatched and maintained study information and supplies ensuring alignment with company processes
• Ensured documents within the electronic trial master file comply with naming guidelines and have the correct status

After starting at Animas through Kelly Services as a lab assistant (see previous experience), I was hired permanently with Johnson & Johnson. My tasks as a lab technician included:- Investigating medical device complaints by utilizing knowledge of electronics, patient data and diabetes- Upholding the quality control standards set by my company according to.

• Animas Corporation is a company which produces insulin pumps with the goal of aiding those with diabetes in managing their disease more easily. At Animas, I:
• Efficiently scan, disinfect, receive and archive an average of 450 insulin pumps per week
• Manage and enter health information data in an environment heavily focused on quality control
• Assist in training new employees on the above tasks

• Provide prompt, friendly customer service to a diverse customer base
• Responsible for stocking inventory, store management and cash accounting
• Organize food label book for customers and update social media websites

University Park, PA, US

• Analyzed molecular differences in bacterial 16S RNA as an independent project
• Assisted in the DNA isolation process through DNA extraction, gel preparation, gel staining, band photography using ChemiDoc, isolation, purification and DNA quantification
• Organized and compiled data for various research projects using Microsoft Office Suite
• Conducted searches of relevant literature in the field and presented the information to stay abreast of developments as well as provided supporting literature for ongoing projects
• Communicated research in weekly lab meetings and the Undergraduate Research Exhibition

Bachelor Of Science (Bs), Biology, General

Bachelor Of Science (B.S.), Biology, General