Sandra Misic

About Sandra Misic

Certified Clinical Research Professional, proactive, self-starter who possesses exceptional multi-tasking and communication skills, both oral and written. Proven communicator with excellent written and verbal speaking and comprehension skills. Thorough, detail-oriented, and able to manage time wisely. Highly organized with good planning and problem-solving abilities. Demonstrate high ethical standards for honesty, truthfulness, and integrity. Knowledge of applicable FDA Code of Federal Regulations, Good Clinical Practices, and ICH guidelines, as well as a detailed understanding of the phases of clinical drug development and clinical operation processes. Ability to receive general instructions on all new assignments and perform routine work with minimal or no supervision. Strong sense of urgency, organizational skills with attention to detail, and ability to follow through on assigned tasks. Proficiency in computer literacy in several software packages, especially Microsoft Office applications (Word, Excel) and database software (eTMF, EDC) to support the operation of clinical trial databases and electronic filing methods. Enthusiastic team player and ability to work effectively in a team/matrix environment Ability to handle multiple tasks and deliver assigned tasks with quality and within specified timelines!

Experience

1. Clinical Research Analyst - Regulatory Affairs Specialist - Neuroscience & Hvr Research Dept

   Swedish

   Jun 2023 — Present · Seattle, WA, US

Education

• Faculty of Law and Business Studies Dr. Lazar Vrkatić

  Bachelor's degree, Foreign Languages, Business, and Linguistics

  2011 — 2016

• Brooklyn College

  Postgraduate Degree, Medical/Clinical Assistant, 3.4 GPA

  2018 — 2022