Walaa Ghitany Phd,Pmp Email & Phone Number

Cairo, Cairo Governorate, Eg

evaluating and assessing the hackathon submissions to determine winners and provide valuable feedback to participants.Offer insights and suggestions to participants to help them refine their projects and presentations

Warsaw Metropolitan Area

Dubai, United Arab Emirates

Cairo, Egypt

• Owner and Founder of Solouk clinic for neonatal diseases.• Diagnosing and Managing pediatric and neonatal diseases.• Review neonatal behaviour and language comprehension.• Examining babies using Brazelton assessment for the first time in Egypt and the middle east.• Established guidelines for monitoring newborns after they leave the NICU and how mothers should handle them.• Assessed numerous cases and wrote some specifications for further action.• Diagnosed several rare genetic and metabolic conditions and monitored numerous rare cases.• Prescribing and administering treatments, therapies, medications, vaccinations, and other specialized medical care.• Directing, coordinating, consulting with, and referring patients to nurses, students, assistants, specialists, therapists, and other medical staff.• Collaborating with HR on hiring new staff members.• Conducting research and remaining up to date on new developments, discoveries, and advances in the field.• Collecting, recording, and maintaining patients' information and histories.

Cairo, Egypt

• Conduct literature reviews and stay up-to-date with the latest developments in pediatric nutrition science.• Develop educational materials for junior doctors about nutrition.

Singapore

data science hands on projects

Cairo, Egypt

Cairo, Egypt

• Evaluate and analyze clinical and non-clinical summaries for regulatory compliance. • Prioritize and submit safety reports to regulatory authorities after a thorough assessment.• Collaborate with the clinical operations team to ensure adherence to local Egyptian regulations for submitting safety information from clinical trials.• Apply sound clinical judgment to identify and include all relevant medical data in adverse event cases and evaluate product safety profiles.• Contribute to developing early clinical strategy by developing protocols, IB, indication selection, study rationale, scientific/clinical endpoints.• Prepare, review, and finalize the medical and scientific portions of clinical study protocols (CSPs), reports, and documents related to trials. • Review and edit documents related to trials, such as monitoring plans, SAPs, amendments, IRB/IEC submissions and regulatory submissions.• Provide medical guidance and review research data for clinical study teams. • Deliver scientific presentations and medical education programs to healthcare professionals.• Ensure compliance of the Clinical Team with ICH GCP guidelines, local regulations, and applicable SOPs regarding participants' safety. • Thoroughly assess and follow up on treated cases to determine the seriousness of reported cases. • Actively contribute to activities relevant to the pharmacovigilance system to ensure safety profile monitoring and regulatory compliance. • Document internal regulatory/PV processes and procedures to support compliant regulatory/PV activities. • Accurately code adverse events using MedDRA for regulatory submission of clinical trials.

• Publish high-quality scientific papers and manuscripts. • Write and compose articles for publication in scientific journals. • Develop materials for Medical Affairs, such as slides and information letters. • Conduct comprehensive research and draft clinical research protocols and study design plans for approval by institutional review boards (IRBs) before commencing research studies. • Research diseases, treatments, or other relevant topics specific to ongoing projects. • Review scientific literature and industry reports to identify emerging trends in research or best practices in treatment methods.

Cairo, Egypt

• Conduct screening of volunteers for over 60 bioequivalence studies, ensuring the recording of all vital signs, body measurements, and demographic data. • Review source documents and CFRs to ensure compliance with regulatory requirements. • Monitor, record, and report adverse events (AE) and serious adverse events (SAE). • Perform and complete case report forms (CRFs) for volunteers, ensuring the accuracy and completeness of data. • Assess risks associated with clinical studies during protocol development and provide insights on risk mitigation. • Manage emergency conditions raised during BE studies and developed corrective action plans to address them.

• Provide leadership and strategic direction to clinical teams and management, overseeing the protocol development process for bioequivalence studies. • Review and analyze scientific and medical data from all phases of clinical research for submission to regulatory agencies. • Expert in managing and organizing clinical data and screening using OpenClinica software, recognized as a key contributor to best practices. • Write and finalize comprehensive study reports for bioequivalence studies, ensuring accuracy and completeness.

Cairo, Egypt

worked as pediatric doctor in school and challenged to control spread of covid-19 between teachers and students after taking these courses (Infection prevention and control for COVID-19 Virus, online WHO course & COVID-19 contact tracing, Johns Hopkins University online course via Coursera, OCT 2020)

Cairo, Egypt

• Develop and create comprehensive research protocols and study designs. • Write thorough literature reviews across diverse medical fields. • Draft detailed scientific data methods, facilitate discussions and prepare manuscripts for publication. • Craft visually compelling and informative infographics for academic and educational presentations.

Online

I work as a judge for technovation for girls competition for judging mobile application done by young girls

Online

Mentoring girls' team for technovation challenge for girls competition, 2017 (drop phone & drive mobile app), 2018 (special needs support app), 2019 (treasury water app) which won 1st place in Africa & granted 1000 $.

Cairo, Egypt

• Diagnose and manage neonatal clinical cases in the neonatal intensive care unit (NICU) and follow-up with patients.• Assess, investigate, analyze, and interpret clinical findings and test results to arrive at a diagnosis, treatment, and reassessment plan.• Prescribe and administer medication, therapy, and other appropriate care to treat or prevent further complications of the disease.• Direct and supervise specialists, residents, nurses, and other medical staff involved in patient care.• Stay up-to-date with the latest research and developments in neonatology and apply this knowledge to provide the highest level of care to patients.

Ai In Healthcare

Artificial intelligence (AI) and cognitive computing are projected to empower patients, transform the practice of medicine. Studying AI.

Diploma, Data Science

Completed 200 hours of data science training diploma, machine learning. Data science uses scientific methods, processes, algorithms.

Doctor Of Philosophy - Phd, Child Health And Nutrition, Excellet

Thesis is about effect of environmental stressor on biobehavioral of admitted neonates in NICU.

Master Of Science - Ms, Pediatrics Residency Program, Very Good

Pediatrics encompasses all aspects of children’s health and wellbeing—physical and mental health, acute and chronic conditions, and child.

Bachelor'S Degree, Faculty Of Medicine, Very Good

Understanding of pharmaceuticals and medical terminology gained through education & clinical experience. Also, monitoring, and assessing.

Data Science Lab, Data Science

Activities and Societies: 8 real projects of data science

Internship, Entrepreneurship & Innovation

Data Analysis

Data analysis with python

Internship, Machine Learning/ Ai

Education record

Activities and Societies: the place where people build cool stuff. 6 weeks program that takes you from idea to 100 users to yourproject

Generative Ai

Activities and Societies: 100 days of how to use AI tools

Ai Tools