Scientist

Haiying Wang

Paramus, NJ *****

201-***-**** *******@*****.***

Career Summary

Working experiences in pharmaceutical industry, academic research, and professional in medical/clinical

practice. Experienced with medical case/report review, case analyses, and critical case evaluation. Trained on

drug adverse events report and fundamentals of US regulatory affairs. Knowledgeable on Good Clinical

Practices (GCP), familiar with medical terminology. Possess necessary medical knowledge and clinical

experience for drug safety and clinical research / trial position. Expertise in:

• •

Clinical Experience, oncology Product Quality Control, cGMP

Selected Accomplishments

Clinical Experience

• Solid medical background with 11 years clinical practice experiences in one of the largest

hospitals in Shanghai, China

• Patient consultation, case historical data / information collection, medical report writing and

reviewing, case monitoring and follow-up

• Drug adverse event recording, side effect complaints severity judgment and management

• Supervised a group of doctors (chief resident, residents, and interns) in the daily clinical

activities

Oncology Solid Tumors

• Specialist on breast cancer and other solid tumors in addition to the most other common

diseases; made diagnosis and treatment plan for patients with cancer and other diseases

• Classroom teaching to medical students on Oncology

• Anticipated general preventive cancer survey that included the early detecting of

tumors in breast, thyroid, and rectum

Quality Control

• Worked in pharmaceutical industry for 10 years on products quality control (QC) under

current good manufacture practice (cGMP) environment

• Experienced in data, protocol, and report reviewing; excellent in problem analyzing

and solving

• Knowledge of drug adverse event (AE) report, clinical trial/monitoring process, and

Good Clinical Practice (GCP)

• Highly motivated and excellent organization skills; Meticulous, detail-oriented with

strong ability in time management

• Sound communication skills both in verbal and writing, in English and Chinese

• Proficient in computer software applications such as Microsoft Word, Excel, etc.

cGMP

• Worked closely with Quality Assurance (QA), regulatory, and compliance group; ensure all

activities are in compliance with FDA regulations and guidelines

• Familiarized cGMP rule, knowledge of FDA regulations and guidelines on drug safety

Haiying Wang page 2

Professional Experience

Pfizer/Wyeth Pharmaceutical, Inc., Pearl River, NY 2002 - 07/2012

Scientist III/II, Department of Quality Control, Chemistry & Biochemistry, Pfizer Specialty-

Biotechnology

• Performed analytical analysis for various vaccine product samples as per established

procedures, such as SOP, STM, and Monograph

• Conducted documentation, review, and approval of test results in both notebook and LIMS;

ensured all the test results meet their specifications or acceptance criteria

• Authored and reviewed SOP, training protocol, analytical report, and job aid

• Training other analysts in analytical assays

• Self-study good clinical practice, drug adverse events and relevant FDA regulations and

guidelines

Kelly Scientific, 2001 – 2002

Temporary position assigned to Dept. of QC, American Home Products Corp., Pearl River, NY

• Performed analytical analysis for vaccine stability and release samples

• Ensured all activities in compliance with cGMP requirements

Xin Hua Hospital, Shanghai Second Medical University, Shanghai, China 1983 - 1994

Attending Physician / Chief Resident / Resident, Department of Surgery

• Clinical practice included daily patient consultant, data collection, physical examination, drug

prescription, advance events management, case report reviewing, critical case management, and

patients follow-up

Related Experience

University of Missouri at Kansas City (UMKC), Kansas City, MO 1999 - 2001

Research Assistant/Associate, Division of Cell Biology and Biophysics, School of Biological Sciences

• Studied the molecular mechanism of signal transduction

Kansas University Medical Center (KUMC), Kansas City, KS 1994 - 1999

Postdoctoral Fellow / Research associate, varied departments

• Studied different projects across various departments included Surgery, Physiology,

Microbiology, Molecular Genetics and Immunology

Education & Professional Training

Bachelor of Medicine, equivalent to Medical Doctor (M.D.) in U.S.

Shanghai Second Medical University

Adverse Drug Events – Understanding and Reporting Requirements

Fundamentals of U. S. Regulatory Affairs

Bioinformatics

Resident, Department of Surgery, Xin Hua Hospital, Shanghai, China

Professional Membership

Regulatory Affairs Professionals Society (RAPS)

Contact this candidate