Binil Benny Email & Phone Number

London, Gb

London Area, United Kingdom

As a Senior Medical Writer at CrowdPharm, I specialize in transforming complex pharmacological data into high-impact regulatory submissions and clinical content for diverse audiences in the healthcare and pharmaceutical sectors. My role involves rigorous data analysis, PK/PD modeling, and content development, ensuring compliance with CDSCO and ICH standards to support marketing authorizations and product safety profiles.Key Achievements and Responsibilities:* Regulatory Submission Excellence: Achieved a 97% approval rate for regulatory submissions by conducting thorough pharmacological analyses and enhancing documentation accuracy, reducing submission errors by 20%.* Data Analysis & PK/PD Modeling: Utilized Monolix for non-compartmental analysis and PK/PD modeling, producing high-quality data that supported client submissions and met rigorous regulatory guidelines.* Safety Communication: Developed Standard Safety Response Letters, including for ADHD treatment Azstarys, integrating clinical and post-marketing data to address regulatory queries and ensure compliance.* Client Project Development: Led the coronary artery disease biomarkers project, enhancing project clarity and reducing scope changes by 18%, resulting in more streamlined and impactful project execution.This role allows me to merge my expertise in pharmacology, data analysis, and regulatory compliance with strategic communication skills, contributing to high standards of scientific integrity and client satisfaction.

Stoke-On-Trent, England, United Kingdom

*Facilitated patient care by closely monitoring vital signs for 8 patients per rotation, leading to a 25% improvement in early intervention rates and achieving a 100% patient satisfaction score.*Coordinated with interdisciplinary healthcare teams to optimize clinical workflow, using Microsoft Access to streamline medical records management, increasing data retrieval efficiency by 20%.*Managed inventory by rotating stock, conducting compliance checks, and checking for expired medications, resulting in a 15% reduction in expired inventory and ensuring regulatory adherence.Influenced patient care decisions by documenting and reporting patient conditions accurately and promptly, which improved communication among healthcare providers and supported patient safety initiatives.*Implemented efficient patient intake processes and conducted education sessions, enhancing the patient experience and reducing intake processing times by 18%.

Birmingham, England, United Kingdom

* Led community-focused cardiovascular health projects, boosting awareness and engagement among local residents.* Coordinated educational outreach, increasing attendance by 25% at cardiovascular health workshops.* Enhanced patient education on lifestyle changes for heart health, helping participants adopt practices that reduced their cardiovascular risk by 15%.* Collaborated with BHF staff to create impactful materials for advocacy events, contributing to a 20% increase in community involvement.

Delhi, India

As a Medical Advisor and Scientific Content Developer at Medical Dialogues, I transformed complex medical data into compelling, accessible content for healthcare professionals. Key achievements included:* Pioneered over 25 SEO-optimized articles and scientific reviews, boosting website traffic by 32% and expanding engagement among clinicians.* Enhanced content shareability by 34%, effectively engaging more than 120 prescribing clinicians within Delhi NCR.* Collaborated across cross-functional teams—including clinicians, pharmacists, and editors—to maintain accuracy and scientific rigor, ensuring adherence to industry standards.* Implemented efficient project management practices using WordPress, meeting client-specific requirements and delivering high-quality content consistently.*Developed scientific communication materials that simplified complex medical data, supporting CME initiatives and enhancing clinician knowledge-sharing.

Moradabad, Uttar Pradesh, India

* Patient-Centered Pharmacology: Consulted with physicians and patients on medication dosages, drug interactions, and disease management. Enhanced patient safety and efficacy with a 39% improvement in patient outcomes by optimizing treatment regimens and implementing therapeutic adjustments.* Data Analysis & Compliance: Conducted PK/PD data analysis, adhering to RECIST criteria to assess trial reliability and efficacy in oncology clinical trials. Improved data accuracy and trial assessment quality, directly supporting therapeutic safety and efficacy across clinical studies.* Precision Medicine Integration: Pioneered the use of Epocrates for the medical team, reducing medication errors by 36% and ensuring rapid access to dosing, contraindications, and drug interactions, which enhanced clinical decision-making and patient care quality.* Stakeholder Communication & Reporting: Created comprehensive patient safety reports and summarized clinical trial data, facilitating clear communication with attending physicians and regulatory bodies. Developed presentations that improved team understanding of trial data, supporting data-driven decisions across departments.* Ethics & Regulatory Documentation: Managed ICF customizations and submissions to the Ethics Committee, ensuring clarity and compliance with regulatory standards. Oversaw ethical review processes to maintain study transparency and participant rights.

Master Of Science - Ms, Pharmacology And Drug Discovery

Activities and Societies: Coventry Research Club, Coventry Student Club, International Student Group, Coventry Sports Club Recent graduate.

Doctor Of Pharmacy - Pharmd, Pharmacology

Activities and Societies: Pharmaceutical society Enrolled in the PharmD program at Teerthanker Mahaveer University, focusing.