Omar Mourad Eissa

Science TeacherFull Time

• Job Details:Plan and deliver engaging and informative science lessons for students in grades 4 and 5 that align with state and national standards. Assess student learning and provide timely and constructive feedback to help students improve their understanding of science concepts. Create and maintain a positive and supportive learning environment where all students feel comfortable asking questions, taking risks, and exploring their interests in science. Collaborate with other teachers and staff to develop and implement effective science curricula and programs. Stay up-to-date on the latest research and best practices in science education. Use a variety of teaching methods and resources to accommodate the different learning styles of all students. Encourage students to be curious and ask questions about the world around them. Foster a love of learning and a passion for science in all students.

CRA III/TLFull Time

• Job Details:Managed a portfolio of clinical research projects, from Phase I to Phase IV, in a variety of therapeutic areas, including oncology, cardiovascular disease, and neurology. Led cross-functional teams of clinical research associates, data managers, and statisticians to ensure successful project delivery on time and within budget. Developed and implemented clinical study protocols, procedures, and strategies. Monitored and reported on project progress to stakeholders, including sponsors, regulatory authorities, and ethics committees. Resolved project issues and challenges in a timely and efficient manner. Key Accomplishments: Successfully managed the launch and completion of a Phase III clinical trial for a new oncology drug, which met all primary and secondary endpoints and is now on track for regulatory approval. Reduced the average time to complete clinical trials by 10% by implementing new project management tools and processes. Improved participant retention rates by 5% by developing and implementing new engagement and support strategies.

CRA IIFull Time

• Job Details:Monitored and reported on clinical trial data and documentation to ensure compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements. Managed relationships with investigators and site staff, providing training and support to ensure high-quality data collection and reporting. Conducted audits and inspections of clinical trial sites to identify and address any potential compliance issues. Escalated serious adverse events (SAEs) to the sponsor and regulatory authorities following GCP guidelines. Mentored and trained junior clinical research associates. Key Accomplishments: Successfully monitored and completed over 20 clinical trials in various therapeutic areas, including oncology, cardiovascular disease, and rare diseases. Identified and resolved numerous compliance issues at clinical trial sites, preventing potential regulatory violations. Mentored and trained over 4 junior clinical research associates, helping them to develop their skills and knowledge