Governor appointed Board member of “New Jersey Advisory Council on Traumatic Brain Injury (TBI)”. Attend meetings to advise the Department of Human Services on issues relevant to brain injury services and TBI fund. Mentor coordinator: Bernards Township Parent for Exceptional Children non-profit organization. Managed, streamlined, and coordinated mentor training for Highschool students for five years. Member of “Brain Injury Alliance of New Jersey”: Attend and provide input to Annual Education Committee. Organized fundraising events for Brain Injury Alliance of NJ and Make a Wish Foundation. Organized a speech on Brain Injury awareness by a distinguished doctor at Rutgers University, NJ. Organized initiatives as a thought leader with key stakeholders involved in the TBI (and general neurological healthcare) research (other parents, physicians, researchers, clinicians, nonprofits, and government entities). Attended the World Stem Cell Summit for several years and has leveraged the role as a patient advocate to develop a deep network of individuals with scientific and legal expertise in the field. Volunteered at Veterans Hospital with a goal to increase public awareness about brain injury. Currently writing a memoir.

Family resource Specialist for five counties in NJ. Work focusses on empowering families with special need child and aiding with their education needs. Worked on Fetal Alcohol Syndrome project and implication of Social Deterrents on Health.

Provide companywide imaging and searching services to proprietary documents. Manage 5 FTE's & 2 contractorsLiaison between Animal Health joint venture initiatives and eDiscovery & Records Management. Migration of Legacy SP preclinical documents to MIDAS Database

Collaborated with Symyx Electronic Laboratory Notebook project as a system administrator. Manage research data to entire Research & Development (R&D) organization, including International sites. Oversee Preclinical Document services to R&D sites. Project Manager for Documentum update. Maintain databases (Notebook, Compound Registration, Preclinical docbase) utilizing SQL developer. Liaison for auditors, regulatory dept, scientists, and legal dept to provide R&D information. Develop R & D Laboratory Notebook Procedure and local Standard Operating Procedures (SOP). Major input to Value Enhancement Initiatives within the company with a savings of $ 5 Million. Successfully implemented satellite areas, increasing customer service (100%), and reducing labor (30%).

Major contributor to Schering Plough Consent Decree commitments. Met FDA project deliverables. Developed training courses and delivered training to third party vendors. Coordinated equipment validation processes (qualification, calibration, and maintenance). Scheduled and managed instrument services with vendors, assuring compliance. Assist in the supplier selection and approval process. Reduced cost control in Metrology area by performing gap analysis (30%).

Contributed to the Zetia data audit for NDA submission report: (Impact Award). Working knowledge of instruments (HPLC, GC, UV/Vis, PDA, IR, Karl Fischer, Cascade Impactor). Developed and validated analytical methods to support NDA/IND. Prepared Stability Reports. Conducted various FDA special studies. Developed protocols for new products. Identified root cause analysis for investigations and resolved technical and non-technical areas. Supervised the purchase, installation, and qualification of laboratory equipment. Project work stream Lead for NJ manufacturing remediation process (Excellence Award). Developed the skills to work independently or as a valued team player.

Instructed Organic Chemistry labs. Responsible for lab safety. Application of HPLC, GC, IR, TLC, UV-VIS, and NMR.