MS, Quality Assurance and Regulatory Affairs
Temple University, Philadelphia, PA
Ferris State University, Big Rapids, MI
Kelly Wright, RPh, MS, is a Senior Associate in the Market Access and Outcomes Strategy group at RTI-HS. Ms. Wright has more than 20 years of pharmaceutical industry experience working in medical and regulatory affairs, medical writing, drug safety and surveillance and drug information. In her role at RTI-HS as technical contributor, she provides research and medical writing support for evidenced-based dossiers, manuscripts, and systematic literature reviews. In addition, in her previous roles in clinical research organizations and the pharmaceutical industry, she was responsible for adverse-event data collection and reporting per regulatory requirements, labeling updates, drug information, and technical writing support for investigational new drugs and new drug applications. Ms. Wright has experience in a wide variety of therapeutic areas, including oncology (e.g., lung cancer, breast cancer and prostate cancer), HIVE, cardiovascular disease, Alzheimer's disease, rheumatology, dermatology, immune and inflammatory diseases, gastroenterology, pain management, female health care, nutraceuticals, infectious disease (including vaccines), and rare diseases (e.g., muscular dystrophy and hemophilia). In addition, she has more than 20 years of experience working as a pharmacist and pharmacy manager in both a hospital and a retail setting. Ms. Wright also has earned Cochrane Collaboration certification in conducting systematic literature reviews.
In her role as project manager at RTI-HS, Ms. Wright is responsible for organizing and preparing materials for project kick-off meetings and ongoing meetings, invoicing clients, maintaining project timelines, and keeping the project team on schedule and within budget. She also is responsible for ensuring that team members comply with Quality Assurance requirements.