Sharon Terry Email and Phone Number

• Manages project designs forNon-Clinical Toxicology integrating developmental plans and project level plans to aide in the support of candidate selection, IND filing and registration. • Monitor toxicology studies at CRO’s for conduct, quality, inspection, accuracy, and timely execution. • Audit raw data for accuracy, review draft reports and finalize them as a submission ready document for regulatory authorities. • Provide response to regulatory authorities in relation to submission approval.• Ensure that supportive study and project related activities are mapped, managed, and ultimately executed.• Write and maintain non-disclosure documents in support of nonclinical activities. • Write and maintain contracts to various contract research organizations for non-clinical support. • Write and maintain statements of work documents. • Work alongside finance to oversee the budget and scheduling of studies, while working to ensure that studies are invoiced correctly prior to payment.

Core Lab Manager: General hospital laboratory functions (e.g. hematology, chemistry, blood bank, microbiology, urinalysis). Oversight of Core Laboratory Staff (Hematology, Chemistry, Urinalysis, Coagulation, Blood Bank)▪ Oversight of 45 direct reports (scheduling, hiring, training, competency, personnel affairs, etc.).▪ Oversight of the Quality Control of all operations in the Core Lab▪ Inspection readiness for Hospital laboratory as well as inspector of various laboratory’s under College of American Pathologists (CAP) standards. ▪ Oversight of Purchasing and projections of capital and non capital items• Member on many hospital and network related meetings (synchronizing laboratory operations across the network of 7 hospitals and numerous clinics)

Pfizer (legacy Wyeth - Drug Safety Evaluation)Reproductive Toxicology Study Director (January 2007 to April 2010)Monitored reproductive and general toxicology studies in laboratory animals on new procedures and/or drug entities. Coordinated the collection of study data (study team members). Performed fetal evaluations and any other procedures on DART and Toxicology studies. Mentored technicians in study design and technical issues.Reproductive Toxicology Project Coordinator (June 1999 to April 2010)Through coordination with senior management and other pertinent groups, assessed resources and studies. Assured availability for specific training requirements, method development and validation processes. Projected metrics and coordinated technical support of study activities and non-study activities (vacations, time reporting, meeting requests). Drafted study protocols and IACUC documents (animal care and use forms) within the group.​Reproductive Toxicology Supervisor (Jan. 1998 to Dec. 2006)Direct, supervised, and assisted technical staff in the conduct of reproductive toxicology studies. Managed direct reports (3 to 7), overall development, performance, discipline, time reporting and work assignment. Trained/mentored new technicians on mastering assigned technical procedures. As a non-GLP principal investigator, planned and interpreted reproductive and developmental toxicology studies in laboratory animals on new procedures and/or drug entities, while ensuring coordination of all parties.Reproductive Toxicology Technician (June 1990 to Jan. 1998)Technical monitor. Administered new chemical entities via various routes (IV, SQ, PO, IP, IM) to laboratory animals according to the study protocol. Observed laboratory animals for toxicological signs and/or behavioral changes and reported observations. Prepared data collection forms, maintained data, and performed quality control utilizing study protocol, facility SOP’s .