Aparna Matpathi

About Aparna Matpathi

I have completed my Doctor of Pharmacy (Pharm.D) at CMR College of Pharmacy, Medchal, Hyderabad. I have done my clerkship and internship at \'Gandhi Hospital,\' Secunderabad, Hyderabad, Telangana, India. During the internship we were trained to identify and monitor adverse drug reactions, drug-drug interactions, and drug-food interactions, providing patient counseling to the patients regarding the disease, medications prescribed, food to be taken, and food to be avoided. I recently became a peer reviewer for the journal titled ‘Journal of Advances in Medicine and Medical Research.’ I have a work experience of a \'Clinical Research Coordinator in AIG Hospitals, Gachibowli, Hyderabad, Telangana, India and I\'m currently working as a Clinical Research Coordinator in Medicover Hospitals Madhapur Hyderabad. The following are my publication details; Publications I published: Research article: Evaluation of Recovery Rate of Poison Patients With or Without Standard Antidote Treatment. Rare case reports: 1. A Rare Case Report of Tyrosinemia Type I 2. A Rare Case Report of Factor IX Deficiency 3. Epidermolysis Bullosa with Severe Anemia in an Infant 4. A Rare Case Report of Guillain Barre Syndrome 5. A Rare Case Report of Iliopsoas Abscess Adverse drug reactions: 1. Terbinafine Induced Steven’s Johnson’s Syndrome Toxic Epidermal Necrolysis Overlap Syndrome 2. Prednisolone Induced Iatrogenic Cushing’s Syndrome 3. Non-Steroidal Anti-Inflammatory Drugs Induced Acute Kidney Injury A Case Report Chapter in a book titled \'Recent Research in Medical and Life Sciences,\' name of the chapter \'Tenofovir Induced Nephrotoxicity.\' Publications I reviewed as a peer reviewer: 1. Hematological Insight: An Epidemiological Study on Anemia Prevalence in Diverse Blood Groups Within the Population of Hyderabad Sindh \"Journal of Advances in Medicine and Medical Research.\" Journals I have been a peer reviewer for: 1. Asian Journal of Research and Reports in Gastroenterology 2. Asian Journal of Research in Nursing and Health 3. Journal of Advances in Medicine and Medical Research 4. B P International

Experience

1. Clinical Research Coordinator

   Iqpads

   Dec 2024 — Present · Hyderabad, IN

   Study Coordination:a) Coordinate schedules for study visits, procedures, and follow-ups to ensure smooth trial progression.b) Manage and oversee clinical trial operations, including participant recruitment, screening, informed consent, and enrollment in compliance with study protocols.2. Regulatory Compliance:a) Ensure all research activities adhere to institutional policies, Good Clinical Practice (GCP), and applicable regulatory standards (e.g, FDA, IRB, and sponsor requirements).b) Maintain up-to-date regulatory documents and submit amendments, progress reports, and safety reports to the appropriate authorities.3. Participant Management:a) Serve as the primary contact for study participants, addressing questions or concerns while maintaining high levels of confidentiality and ethical standards.b) Monitor and ensure participants’ safety, adherence to the protocol, and accurate reporting of adverse events or deviations.4. Data Collection and Documentation:a) Accurately collect, record, and input research data into designated databases or electronic data capture (EDC) systems.b) Perform regular quality checks to ensure data integrity and compliance with study protocols.5. Liaison Activities:a) Act as a central point of communication between study sponsors, investigators, healthcare providers, and regulatory bodies.b) Coordinate and facilitate monitoring visits, audits, and inspections, addressing any findings promptly.6. Operational Support:a) Manage study supplies, including procurement and inventory of investigational products, lab kits, and other research materials.b) Assist in the development and revision of study-related documents, such as standard operating procedures (SOPs), protocols, and informed consent forms.7. Report Preparation and Analysis:a) Generate accurate and timely reports for investigators, sponsors, and regulatory authorities.b) Participate in data analysis, preparation of manuscripts, and presentations as required.

Education

• CMR College of pharmacy

  Doctor of Pharmacy - PharmD

  2017 — 2023