Vesna Stanisic

• Developed and strategized comprehensive treatment plans for complex cases based on their medical history and current condition through collaboration with the team.
• Provided scientific information and presented case studies to educate physicians on rare syndromes and differential diagnostic challenges.
• Educated patients and their families on various pediatric and neurological conditions and available treatments, delivering presentations during bi-weekly online meetings.
• Developed and delivered personalized and focused online sessions regarding a patient's condition or treatment plan to family members and explained potential diseases or traumatic conditions prognoses.

• Developed training curriculum for pediatric neurology techniques implementation focusing on physicians.
• Supervised and trained attending neurologists in pediatric neurology techniques and approaches to children.
• Developed, strategized, and executed treatment plans for complex cases through collaboration with the team.
• Provided scientific information and presented case studies to educate physicians on rare subjects based on Real World Evidence Studies.

• Interviewed, examined, and treated 12+ pediatric neurological patients daily to support cognitive and physical development and prevent complications caused by primary diseases.
• Educated patients and their family members on various neurological conditions' treatment and provided care.
• Supported patient advocacy groups by providing scientific data and encouraging official dialog with the government by representing patients and their families during campaigns.
• Developed and delivered presentations and case studies on various neurological and cross-sectional subjects at international conferences and congresses.

THERAPEUTIC AREA EXPERIENCE (Phase II-IV): Neurology – Chronic Back Pain, Headache, Malignant Pain Management, Multiple Sclerosis, Parkinson’s Disease, Surgery- Postoperative Pain Management, Oncology-Chronic Pain Management in Malignancies

• Evaluated participants’ eligibility for the clinical trial and approved subjects for admission to the study
• Ensured site compliance with study protocols, standards of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), quality (QA/QC) procedures, and local authority regulations
• Evaluated the safety and efficacy by reviewing and analyzing data, recording outcomes of the intervention, and assessing the safety profile
• Reviewed, investigated, and reported adverse events (AE), and serious adverse events (SAE) and completed causality assessments
• Provided medical management of adverse events based on the research protocol
• Monitored the site participation in trials and completed all study documentation per the study-specific requirements
• Collaborated with healthcare professionals and sponsors on study conduct and execution as required by regulatory authorities

• Prevented and treated various diseases in children and adults, attending to approximately 60 patients per day by taking permanent care of 3450 assigned patients, based on guidelines for good scientific practice and use of the EDC recording
• Developed, prescribed, and delivered treatments and other specialized medical care to diverse patient groups on an everyday basis while focusing on patients' primary disease management
• Managed and monitored outpatient center activities and supervised 20 people to satisfy customers' needs and address health problems
• Successfully designed educational materials, managed and executed public campaigns to increase awareness about the community’s health problem

• Conducted more than 1000 interviews in multiple languages by generating clinical and scientific data and conducting quality checks to ensure data integrity, implementing edit checks, performing validation procedures, and resolving data discrepancies promptly to maintain high-quality databases
• Regularly updated and maintained databases in academic settings, including version control, data archival, and documentation of database changes
• Interpreted and analyzed clinical and scientific data to enhance adequate responses to recent COVID-19 outbreaks
• Collaborated with other CICT/CORG-EDU team members by presenting cases, reviewing regulatory guidelines, and recent COVID-19 outbreaks, and proposing strategic plans for adequate responses to recent COVID-19 outbreaks

• Managed ongoing and outgoing correspondence for the Neonatal Intensive Care Unit, Pediatric Development Center, and Oncology/Hematology/Geriatric Unit 541.

• Provided nuanced understanding of clients' health issues based on scientific investigation.

• Provided comprehensive support for the project "Woman Can Do It" and the sub-projects "Women in Focus," coordinated by the Voice of Difference and Women's Political Network, the NGO "PAZ," "HORA," and "Hourglass" and supported by the Norwegian People Aid (NPA).
• Collaborated with the working group for gender equality of the Stability Pact and Organization for Security and Cooperation in Europe (OSCE).
• Conducted seminars, designed, and executed local campaigns with women leaders in Western and Central Serbia and Vojvodina in the field of gender equality with the primary goal of empowering them to take active participation in creating political and public life.

• Designed and implemented campaigns to sensitize the local community regarding mental health issues, focusing on suicide in the city of Nis.

• Led a team of 35 high professionals and 200 volunteers based on cross-functional leadership strategies.

• Organized debates, tribunes, and round tables with different topics (anxiety, depression, suicide) on local TV and radio stations with prominent health professionals as guests (psychiatrists, psychologists, social workers)

The most successful was the campaign "Stop to Suicide," which resulted in permanent multidisciplinary team formation and decreased the suicide rate by 36% in the next three years.