Shijie (Jason) Mao, Pharmd Email & Phone Number

Boston, Massachusetts, US

Boston, Massachusetts, US

Served as the lead Rare Oncology Medical Reviewer for Global and US Materials

Served as the Subject Matter Expert (SME) for Genitourinary Oncology products.

Served as the Subject Matter Expert (SME) for Infectious Diseases and Transplantation products

• Developed standard response letters (SRLs) in preparation for AVXS-101’s product launch including topics of adverse reactions (AEs), drug interactions, onset of action, and dosing among others
• Led internal training and budgeting assignments for Copyright Clearance Center’s RightFind system used for literature and permission requests
• Managed and distributed biweekly literature alerts on relevant topics such as gene therapy, spinal muscular atrophy, and Rett syndrome
• Conducted primary medical reviews of SRLs developed for AVXS-101
• Educated healthcare providers (HCPs) regarding AveXis’ science and pipeline while staffing the Medical Information booth at the 2019 Child Neurology Society (CNS) meeting
• Developed and communicated appropriate and timely responses to medical inquiries from healthcare providers and consumers with documentation using IRMS

Claremont, CA, US

• Led Keck Graduate Institute’s 12-week Advanced Pharmacy Practice Experience (APPE) for pharmaceutical/biotechnology industry rotation
• Completed longitudinal research project on pharmaceutical industry clinical trials utilizing gene therapy with poster presentation at ASHP Midyear Meeting
• Completed the ASHP Teaching Certificate for Pharmacists

Woonsocket, Rhode Island, US

• Provided immunizations, medication counseling, medication compounding, medication reconstituting, and drug interactions counseling for patients
• Assisted patients with medical questions and concerns under the supervision of a pharmacist
• Worked with other health professionals including nurses, doctors, physician’s assistants, pharmacists, other technicians, and patients

Richmond, VA, US

• Assisted in the construction of a clinical study protocol, pharmacy manual, and Request for Protocol for a subcutaneous buprenorphine (RBP-6000) study
• Analyzed prior studies on subcutaneous buprenorphine (RBP-6000) along with primary literature to project clinical supplies required for the impending RBP-6000 clinical trial
• Collaborated cross-functionally to create the Protocol Review Forum for internal protocol and safety review
• Supported the pharmacokinetic study protocol development for subcutaneous risperidone (RBP-7000) by reviewing and summarizing literature on oral risperidone

New York, New York, US

• Supported research for product development and formulations of Preparation-H and Nexium. Studies included: solubility studies, stability studies, and experimental design
• Utilized techniques and equipment such as emulsion technology, developmental stability studies, consumer studies, HPLC, monolithic tablet manufacturing, patent reviews, monograph reviews, polarized microscopy, specific.
• Completed and presented a summer project on the resolution of a precipitation issue with a Preparation-H formulation in a technical presentation to Pfizer scientists and other employees

Richmond, VA, US

• Conducted a study in the Department of Pharmaceutics for identifying the structure of the human organic cation transporter (hOCT) protein by mutating OCT2 and performing uptake testing
• Prepared and presented a research poster detailing experimental methods and results obtained
• Utilized techniques such as mutagenesis, sub-cloning, scintillation, cell culture, stable cell line establishment, transfection, uptake experiments and km testing

Doctor Of Pharmacy (Pharmd)

Bachelor'S Degree, Biology/Biological Sciences, General