Hello! I’m a former pediatric clinical pharmacist with a strong passion for clinical research. Throughout my hospital career, I focused on applying new research to enhance patient outcomes. Since transitioning to the industry, my enthusiasm for contributing to the process of bringing medications to market has only grown. I’ve gained extensive experience collaborating with healthcare providers and cross-functional teams in every role I’ve held so far.

Mercer University

The George Washington University

\-     Identify, select, initiate, and close-out appropriate investigational sites for clinical studies
\-     Monitor sites in order to ensure that studies are carried out according to the study protocol and the principles of ICH-GCP
\-     Proactively identify Protocol Deviations, communicate a CAPA plan to the study team, and provide re-training to the site based on identified areas of improvement
\-     Remain compliant with monitoring plans and study timelines utilizing various systems, resources, and training provided by the study team and Sponsor
\- Provide a benchmark of monitoring competence to inexperienced / less experienced colleagues

Clinical Research Associate II

\-     Provide monitoring visits and site management for a variety of protocols, sites, and therapeutic areas
\-     Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
\-     Evaluate the quality and integrity of study site practices ensuring regulatory, ICH-GCP, and protocol compliance
\-     Manage the process of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form completion and submission, and data query generation and resolution
\- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation

Clinical Research Associate

\-     Review complex medical literature to create institution-specific practice guidelines and incorporate clinical work processes in Epic

*   Developed guidelines and ordering functions in Epic that decreased antibiotic utilization by greater than ten percent in newborn nurseries and neonatal intensive care units across three hospitals within the health-system

\-     Support provider group and multiple hospitals within the health-system for all projects in the neonatal intensive care unit (NICU) including evaluation of safety outcomes for guidelines and protocols

*   Reviewed policies and standard operating procedures to ensure compliance with regulatory standards

\-     Inform various audiences of population expertise

*   Formulate content using PowerPoint and present neonatal topics at local and regional conferences
*   Answer multiple drug information questions for providers across 5 different institutions within the health-system

\-     Partner with multiple sites within the health-system to enhance and standardize processes and safety features

*   Implemented complex projects that link the electronic health record to smart pumps
*   Coordinated a multidisciplinary team to create a standard protocol for neonatal withdrawal syndrome across three hospitals within the system that led to decreased length of stay and treatment days
*   Standardized over fifteen processes amongst four local sites within the neonatal intensive care units
*   Standardized neonatal and pediatric smart pump medication libraries across the health system in preparation for interoperability

\- Train and mentor students, residents, and new hire pharmacists

Clinical Pharmacist Specialist

\-     Obtained IRB approval for research regarding antibiotic dosing in the neonatal intensive care unit resulting in site practice changes to initial dosing based on pharmacokinetic parameters

*   Presented research at a national pediatric conference

\- Implemented use of dextrose gel in the newborn nursery leading to decreased neonatal intensive care admissions

Pharmacy Practice Resident, Post Graduate Year-2

\-     Obtained IRB approval for research to assess vancomycin dosing practices in the pediatric population resulting in site specific practice changes with initiation and escalation of doses
\-     Devised a medication use evaluation quality improvement project to assess appropriate indications for Kcentra® based on ordering history leading to expanded criteria for use

*   Presented findings at a regional conference

\-     Requested addition of medications to formulary through Pharmacy and Therapeutics Committee leading to > $16,000 cost-savings
\- Presented a local and regional continuing education topic that led to a change in dosing practice and savings of thousands of dollars

Pharmacy Practice Resident, Post Graduate Year-1

\-     Identified and reconciled over twenty medication-related problems daily
\-     Assessed and interpreted scientific literature answering complex drug information queries from health-care providers
\- Reviewed and revised over five student medication-use evaluation abstracts for poster submission

Clinical Pharmacist

Roshni Patel

English

Communication Skills

Networking

Data Analysis

Critical Thinking.

Strong attention to detail with the ability to handle multiple tasks simultaneously and with precision

Product knowledge

Problem Solving

Relationship Building

Public speaking

Regulatory requirements (FDA)

PowerPoint presentations

Research skills

Strategic Thinking

medical education

Competitive

Scientific Communication

Clinical Expertise

Disease State Knowledge

Kol Management

Communication

Conflict Resolution

Emotional Intelligence

Leadership

Time management

Ability to adapt to rapidly shifting priorities in fast-paced environment, including switching between multiple task/projects in the same day

Roshni Patel

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