Dr Cynthe Sims received a Ph.D. in Chemistry from Texas Tech University where she was the recipient of numerous awards, notably, twice awarded National Science Foundation GK-12 Fellowship.
Dr Sims is a Board-Certified Clinical Laboratory Director- HCLD(ABB) with over 10 years of experience in both technical and management roles focusing on molecular diagnostics and precision medicine. She joined InnovativeGx in the fall of 2020 as Clinical Laboratory Director. She also serves as Laboratory Director for several domestic and international clinical laboratories.
Dr Sims participates in many professional and volunteer activities including service as a CAP volunteer inspector, CLSI guideline committees and as a mentor at San Diego State University. Originally from Texas, she has resided in San Diego, CA since 2012.
Margo Lee is a career geneticist and biotechnology specialist with 25+ years of experience supporting international efforts in genetic / biotechnology research, development, and FDA regulatory process and compliance. Strong foundation in scientific research with advanced training and specialties in the genetic basis of disease, DNA sequencing, infectious disease, protein assays, stem cell research and applications, whole-genome sequencing (WGS), and pharmaceutical research. Serves as expert counsel for customers, field sales, and laboratory staff, as well as chief advisor for company board members on the direction of research and development, current events in clinical trials, laboratory management, and hiring of employees.
Pejman Rahimian is a Scientist, diagnostic laboratory consultant and educator with 14+ years of experience in Microbiology, Molecular Diagnostics, and Immunodiagnostics. His expertise is in assay development and validation as well as supervision and operation of high-complexity CLIA laboratories.
Sally Camacho has conducted Graduate Scientific Research, conducting literature reviews, collect and analyze data, prepare materials for submission to granting agencies and foundations, maintain accurate records of interviews, safeguarding the confidentiality of subjects,and attend project meetings. Demonstrate strong organizational skills to ensure thorough information tracking in material management systems associated with antibody development and production. Attend area seminars and other meetings as necessary, summarize project results, prepare progress reports for the PI and funding agencies, prepare other articles, reports, and presentations including all experimental data.
Perform complex technical work involving molecular analysis of human biological materials. Job duties include a combination of the following responsibilities: extensive and complex steps requiring manual
manipulation and pipetting, close monitoring and control, evaluation of
data, and careful and accurate work.