CAMBRIDGE, Mass.--(BUSINESS WIRE)--PROMETRIKA, LLC has announced that Susan Boquist has joined their Statistical Programming team as Associate Director. Ms. Boquist brings to this position over 20 years of diverse experience including leadership roles in statistical programming, data standards implementation, and clinical database design.
At PROMETRIKA, Susan will direct statistical programmers in the design, implementation, and quality review of programming to support statistical analyses of trial data. Susan will contribute her expertise in CDISC SDTM and CDISC ADaM standards to further enhance PROMETRIKA’s delivery of best-in-class clinical research.
“Susan’s experience and leadership skills are a significant addition to our company,” commented Miganush Stepanians, President & CEO. “As a leader in statistical programming, she has excelled at developing highly-skilled programming teams exhibiting the flexibility necessary in today’s biotechnology and pharmaceutical development space. Susan’s deep and wide knowledge as a SDTM subject matter expert will further enhance PROMETRIKA’s leadership in the area of data standardization and electronic data submissions to regulatory authorities.”
Ms. Boquist’s prior leadership roles have included Senior Manager of Statistical Programming and Associate Manager of Clinical Database Programming at PAREXEL International Corp. Her work has covered studies in a variety of therapeutic areas including oncology, infectious disease, anesthesiology, and allergy/immunology. She has also been a team member on several successful FDA and PMDA new drug submissions.
“I am excited to join this growing and innovative full-service CRO,” said Ms. Boquist. “This is a tremendous opportunity for me to bring both my professional experience in CDISC implementation and my leadership experience developing teams with a constant eye on collaboration, process improvement, and training.”
Ms. Boquist received her Bachelor of Arts (Psychobiology) degree from Mount Holyoke College.
About PROMETRIKA, LLC - www.prometrika.com
Founded in 2003 and based in Cambridge, Massachusetts, PROMETRIKA is a unique Clinical Research Organization (CRO), utilizing a collaborative approach to clinical development and execution with a close-knit, highly-experienced senior leadership team involved in all phases of trials. PROMETRIKA’s services include complete clinical operations and clinical trial management, data management, pharmacovigilance, biostatistics and programming, medical writing, and regulatory submissions.