sajeela shahzad

Handled sensitive clinical and technical data, ensuring all regulatory documentation complied with internal SOPs, sponsor-specific confidentiality, and international regulatory standards (e.g., FDA, ISO 14155). Prepared and managed essential clinical trial documents, including Clinical Investigation Plans (CIP), Informed Consent Forms (ICFs), Clinical Study Reports (CSRs), and regulatory submissio

Researched and wrote evidence-based articles on aging, cognitive health, and medical topics, ensuring accuracy and clarity for a broad audience. Translated complex medical and pharmacological concepts into engaging, reader-friendly content to educate seniors, caregivers, and healthcare professionals. Optimized content for SEO and digital marketing strategies, increasing reader engagement and acces

Engaged in medical writing projects under the supervision of senior medical writers, gaining hands-on experience in various aspects of medical content creation. Conducted thorough research on medical topics, synthesized information from diverse sources, and drafted content for scientific articles, promotional materials, and educational resources. Assisted in reviewing and editing medical documents

Created and edited high-quality medical content, including research articles, blogs, and patient education materials, ensuring scientific accuracy and clarity. Collaborated with researchers, clinicians, and editors to translate complex medical data into accessible and engaging narratives for a broad audience. Conducted literature reviews and fact-checking to support evidence-based writing aligned

Collaborated with healthcare teams to optimize patient outcomes through medication therapy management and patient assessments. Prepared customized medications from raw materials and ensured prescription safety by assessing for appropriateness, drug interactions, and adverse effects. Actively participated in multidisciplinary rounds and engaged in quality improvement initiatives, serving as a key d

Activities and societies: Participated in Continuing Medical Education (CME) from WHO, Stanford, George Washington, and Harvard, covering topics like pandemic diseases, antibiotic stewardship, and diabetes. Gained research experience supporting compound purification, drug formulation, and conducting synthesis and behavioral pharmacology studies using preclinical rodent models.

Completed a Doctor of Pharmacy (Pharm-D) program. Focused on pharmacotherapy, with a dissertation on “Pharmacotherapy of Stroke.”