Summary
Overview
Work History
Education
Skills
Publications
Languages
Short term Course - Emergency Medicine
Certification
Timeline
Generic

Bhavitha Sri Muppalla

Fairborn,OH

Summary

Detail-oriented and motivated Clinical Research Coordinator Intern with hands-on experience as a Clinical Pharmacist Intern. Proven ability to support clinical trials, ensure regulatory compliance, and maintain data integrity. Strong background in patient care, medication management, and healthcare team collaboration. Skilled in conducting research, managing patient recruitment, collecting and analyzing clinical data, and supporting research protocols. Passionate about advancing medical research and improving patient outcomes through evidence-based practices. Seeking to leverage pharmacy expertise and clinical research knowledge to contribute to high-quality, impactful clinical trials.

Overview

2
2
years of professional experience
1
1
Certification

Work History

Clinical Research Coordinator Intern

Wright State Physicians Inc.
Fairborn, Ohio
08.2024 - Current
  • Compiled trial related documents into a master file as required by sponsor or regulatory agency.
  • Assisted in preparing periodic reports summarizing progress of clinical studies.
  • Performed patient assessments, collected and analyzed data, and prepared reports.
  • Monitored patient safety during clinical trials according to established guidelines.
  • Provided guidance on Good Clinical Practice regulations and other applicable regulatory standards.
  • Coordinated investigator meetings, conference calls, and site initiation visits as needed.
  • Collaborated with internal departments such as Regulatory Affairs and Data Management to ensure that all studies were conducted in accordance with ICH-GCP guidelines.
  • Reviewed CRFs for completeness and accuracy before database entry.
  • Prepared informed consent forms for review by ethics committees.
  • Kept patient care protocols and clinical trial operations in compliance.
  • Adhered to standards in areas involving data collection, research protocols, and regulatory reporting.
  • Monitored subject enrollment and tracked dropout details.
  • Took vital signs and collected medical histories as part of study protocols.
  • Conducted screening interviews to determine eligibility of possible subjects.
  • Educated participants on studies and anticipated outcomes.
  • Assisted in the development of marketing materials, such as brochures, flyers, and promotional items.

Clinical Assistant Internship

Manipal Hospitals
India, Andhra Pradesh
07.2022 - 07.2023
  • Evaluated and reported adverse drug reactions and medication errors to regulatory agencies.
  • Maintained up-to-date knowledge of pharmacology, therapeutics, and new drug developments.
  • Provided pharmacokinetic consultations to optimize dosing regimens for individual patients.
  • Counseled patients on drug therapies to ensure proper intakes.
  • Answered patient questions and data requests.
  • Conducted patient interviews to gather health history, vital signs, and information about current medical issues.
  • Reviewed patient medical records for drug allergies, interactions, and contraindications to ensure safe medication use.
  • Conducted regular reviews of medication profiles to identify possible adverse reactions or duplications in therapy.
  • Maintained a current knowledge base of pharmaceuticals through continuing education activities and literature review.
  • Investigated drug information requests from health care providers including indications, dosing regimens, contraindications, interactions, adverse reactions.
  • Performed quality assurance audits on prescriptions dispensed to ensure accuracy of dosage forms and directions for use.
  • Provided counseling to patients regarding their medications including appropriate administration techniques as well as potential side effects or allergic reactions that may occur.

Education

Master of Science - Pharmacology and Toxicology

Wright State University
Dayton, OH
12-2024

Doctor of Pharmacy - Pharmacy

Acharya Nagarjuna University
Andhra Pradesh, India
08-2023

Skills

  • Informed consent
  • Patient recruitment
  • Adverse event tracking
  • Study protocols
  • Protocol development
  • Participant screening
  • Good clinical practice
  • Participant recruitment
  • Scheduling proficiency
  • Dispensing oversight
  • Medical terminology proficiency
  • Patient-focused care
  • Patient education and counseling
  • Drug utilization review
  • Dosage requirements
  • Treatment monitoring
  • Error prevention
  • Drug utilization evaluation
  • Quality improvement initiatives

Publications

  • A comparative study on assessment of adverse drug reactions among different types of cancer chemotherapy patients in a tertiary care hospital.
  • Assessment of Chemotherapy-Related Adverse Drug Events And Toxicities In Cancer Patients.

Languages

English
Professional
Telugu
Native/ Bilingual

Short term Course - Emergency Medicine

Trained and experienced in handling emergency medicine related to basic life support and advanced life support procedures

Certification

  • CITI - Conflicts of Interest
  • CITI - Responsible conduct of research
  • CITI - Good Clinical Practice and ICH
  • CITI - Human Research
  • ACRP - introduction to clinical trials
  • Mayo Clinic Laboratories - Dangerous Goods Training
  • Lean Six Sigma White Belt
  • Lean Six Sigma Green Belt

Timeline

Clinical Research Coordinator Intern

Wright State Physicians Inc.
08.2024 - Current

Clinical Assistant Internship

Manipal Hospitals
07.2022 - 07.2023

Master of Science - Pharmacology and Toxicology

Wright State University

Doctor of Pharmacy - Pharmacy

Acharya Nagarjuna University
Bhavitha Sri Muppalla