ASIF SHAIK
LODI,USA
Summary
Results-oriented Health Informatics professional with a Master's degree and hands-on experience in analyzing and interpreting healthcare data. I am adept at developing robust information management systems and proficient in using electronic medical record (EMR) and Electronic Health Care Record (EHR) systems. Skilled in implementing data visualization tools and leveraging statistical software to derive actionable insights. Passionate about contributing to the evolution of healthcare through innovative informatics solutions and staying abreast of emerging trends in the dynamic field of Health Informatics.
Overview
3
3
years of professional experience
1
1
Certification
Work History
Clinical research coordinator
DM Clinical Research
NJ
11.2024 - Current
- Coordinate and manage clinical trials in compliance with applicable regulations and standard operating procedures (SOPs)
- Conduct Source Document Review of appropriate site source documents and medical records
- Have interacted directly with the Clinical team (e.g., CRAs, managers), site staff, and vendors to provide support in project-specific tasks and the overall management of clinical trials
- Records adverse event and side effect data and confers with investigators regarding the reporting of events to oversight agencies
- Prepares for or participates in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups
- Identifies protocol problems, informs investigators of problems, or assists in problem resolution efforts such as protocol revisions
- Keep abreast of SOPs, Good Clinical Practice (GCP), ICH guidelines, state and federal laws, and ethical standards
- Writing clinical trial documentation for a pharmaceutical company analyzing the efficacy of a new antidepressant, including consent forms, study protocols, and QC guidelines
- Coordinating the day-to-day activities of the research study team specifically engaged in carrying out the research clinical protocol
Clinical Research Coordinator
ASMORS Public General Hospital
Guntur, India
07.2022 - 07.2023
- Part of the 'Covaxin Phase 3' study, responsible for electronic data capture of over 1000 enrolled patients
- Coordinating, actively recruiting, and formally consenting study subjects for enrolment
- Preparing research study advertisements submission to the institutional review board (IRB) for approval aid in recruitment
- Performing input, retrieval, and analysis of data for processing and validation, and maintaining research databases on Excel
- Participated in the 'Hepatitis C Phase 3' study, managing site master files, documentation, and IP management
- Volunteered in the 'National Viral Hepatitis Control Program' to create patient awareness
- Conducted interviews, sent out questionnaires, and recorded research interventions and participant medical data
- Assisted in developing and implementing study protocols, ensuring compliance with ethical guidelines
- Coordinated and managed clinical research projects, ensuring adherence to study protocols
- Played a key role in optimizing workflow processes, ensuring efficient coordination among team members
- Acted as a liaison between study sponsors, principal investigators, and study participants
- Contributed to the preparation of study reports, manuscripts, and presentations for scientific conferences
- Assisted in patient care, prescription monitoring, and medication management
- Collaborated with healthcare professionals across diverse departments
- Managed medical records, health insurance, and administrative tasks
Education
Master of Science - Health Informatics
Sacred Heart University
Fairfield, CT, USA12.2024
Bachelor of Pharmacy -
Chalapathi Institute of Pharmaceutical Sciences
Guntur, A.P, INDIA07.2022
Skills
- Therapeutic and medical areas
- Scientific data retrieval
- Data-capturing software
- MS Office
- SAS
- SQL
- Tableau
- Critical thinking
- Leadership
- Time management
- Integration
- Research
- Electronic Medical Record (EMR) systems
- Case report management
- Research experience
- Trial management
- Clinical research ethics
- Laboratory results management
- Study protocols
- Informed consent
- Good clinical practices
- Meeting coordination
- Clinical trial management
- Good clinical practice
Certification
- Good Clinical Practice, NIDA
- Registered Pharmacist
Projects And Publications
- Impact of Clinical Pharmacist Intervention on Post-Stroke Follow-up Patients.
- Case report on oral corticosteroid-induced Malassezia folliculitis.
- Capstone Project: Implementation of Electronic Health Records (EHR) Systems Affect the Quality and Cost of Patient Care in Rural Healthcare Facilities, Sacred Heart University, USA, Conducted in-depth research on the impact of EHR implementation on patient care quality and cost efficiency in rural healthcare settings. Analyzed data to evaluate improvements in clinical workflows, patient outcomes, and financial sustainability post-EHR adoption. Identified key challenges and provided recommendations for optimizing EHR integration to enhance healthcare accessibility and operational efficiency. Assessed barriers such as infrastructure limitations, provider adoption challenges, and interoperability issues in rural healthcare facilities. Presented findings and actionable insights to healthcare professionals and academic faculty, demonstrating expertise in health informatics and data-driven decision-making.
- Anti-Diabetic Polyherbal Formulation, Chalapathi Institute of Pharmaceutical Sciences, Guntur, INDIA, Designed and developed a polyherbal formulation aimed at diabetes management as part of undergraduate research. Conducted preclinical trials to evaluate the safety and efficacy of formulation on human subjects, adhering to ethical guidelines and regulatory standards. Performed laboratory experiments and analyzed data to ensure the formulation's stability and therapeutic potential. Gained hands-on experience in research methodologies, herbal formulation techniques, and preclinical trial protocols. Documented findings and collaborated with a team to prepare a comprehensive project report.
Timeline
Clinical research coordinator
DM Clinical Research
11.2024 - Current
Clinical Research Coordinator
ASMORS Public General Hospital
07.2022 - 07.2023
Master of Science - Health Informatics
Sacred Heart University
Bachelor of Pharmacy -
Chalapathi Institute of Pharmaceutical Sciences