Camila G.

Study Administrator | Clinical Trials & Observational Studies | RWE

Professional with a bachelor's degree in Nursing from UFRGS, PhD and Master's degree in Health Sciences from the Medicine College-UFRGS, and over 10 years of experience in different fields of clinical research and scientific advisory. Demonstrates solid skills in clinical study and data management, including RWE and RWD, SR, ECR, compliance with regulations and good clinical practices, including IRB/IEC submissions and informed consent form adequacy. My experience includes expertise in study coordination, study design, scientific publication, assessment of instrument accuracy including Patient Reported Outcome Measures (PROMs) and Patient Reported Measures (PREMs), electronic Clinical Outcome Assessments (eCOAs) development, contract review and negotiation, and development of feasibility strategies for clinical study proposals, providing scientific support to legal sectors and to internal and external teams, including sites, CROs and the pharmaceutical industry. Additionally, I have worked as a lecturer and scientific consultant, enhancing my communication, training, and technical support skills, which are essential for collaborating with multidisciplinary teams and for easily capturing the different needs of professionals, translating them into scientific studies. Through my experience as an independent scientific consultant, I developed an entrepreneurial vision and leadership skills, offering customized solutions to different healthcare needs, including various therapeutic areas. I am dedicated and self-disciplined, with a capacity for fast learning. I am excited about the opportunity to apply my experience and knowledge in a dynamic and collaborative environment where I can learn, grow, and add significant value.