Organized and dependable candidate successful at time management and multitasking. Managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.
Overview
15
15
years of professional experience
Work History
Reporting Associate I
Syneos Health
12.2017 - 05.2023
Independently composed scientific reports for validations and clinical studies in compliance with appropriate protocols, SOP's and regulatory agencies in a timely, efficient, and quality manner.
Responsible for compiling and interpreting scientific data to prepare data tables that were included in report.
Completed reports were utilized by large pharmaceutical companies for submission to regulatory agencies.
Managed innumerable emails and calls daily.
Direct communication with clients.
Provided support for specific requests received from clients.
Provided quality control review of documents written by peers.
Maintained report templates required for report writing activities.
Electronically archived reports and data.
Supported quality assurance efforts by meticulously reviewing documentation for completeness and compliance with company standards.
Study Coordinator I, Bioanalytical Chemistry
Covance Laboratories, Inc.
11.2015 - 11.2017
Independently performed activities related to project management.
Coordinating activities for routine scientific studies in compliance with protocols, standard operating procedures and regulatory agency guidelines in a timely, efficient, and quality manner.
Drafting scientific reports and data tables.
Performed peer review, complied data transfers and data transfer review.
Reviewed and addressed report and data audits in a timely manner.
Interacted with clients and colleagues in a professional manner.
Quality Assurance Officer, Quality Assurance
Tandem Labs
06.2015 - 11.2015
Enhanced product quality by implementing rigorous testing procedures and protocols.
Reduced defect rates through meticulous inspection processes and root cause analysis.
Achieved customer satisfaction with thorough audits of products, ensuring adherence to standards.
Improved manufacturing processes by identifying areas of inefficiency and recommending corrective actions.
Collaborated with cross-functional teams for timely resolution of quality issues and concerns.
Maintained a high level of expertise in quality assurance processes through ongoing professional development and staying abreast of industry trends,
Quality Control Microbiologist
The American Red Cross
11.2008 - 02.2013
Enhanced product quality by conducting rigorous microbiological testing and analysis on raw materials and finished products in compliance with FDA and GLP regulations.
Implemented effective corrective actions for non-conforming products, resulting in reduced rework and waste.
Assisted in streamlining laboratory processes, leading to improved efficiency and turnaround time for results.
Conducted immediate action on out of specification testing results including investigation, repeat analysis and confirmation.
Education
Bachelor of Arts - Biology
Arcadia University
Glenside, PA
05.2007
Skills
Excellent time management and multi-tasking skills
Senior Lead Project Specialist – Global Clinical Trials & RWLP at Syneos HealthSenior Lead Project Specialist – Global Clinical Trials & RWLP at Syneos Health