Summary
Overview
Work History
Education
Skills
Certification
LANGUAGES
Timeline
Generic

Gurinder Takhar

Middletown,DE

Summary

Professional with experience in clinical research coordination, equipped to make significant impact in this field. Demonstrated ability to manage clinical trials, ensure compliance with protocols, and maintain accurate documentation. Strong emphasis on team collaboration, reliability, and adaptability to evolving project requirements. Proficient in patient recruitment, data collection, and regulatory submissions, with results-driven approach that ensures successful study outcomes.

Overview

11
11
years of professional experience
1
1
Certification

Work History

Clinical Research Coordinator

05.2023 - 05.2025
  • Maintain a working knowledge and ensure compliance with ICH-GCP guidelines, local regulatory requirements, SOPs, and study specific procedures
  • Expertly conduct full range of patient and protocol assessments including, vital signs, EKGs, PFTs, etc.
  • Actively contribute to meetings with sponsor/CRAs, sharing value study data and insight as requested
  • Communicate effectively and efficiently to principal and sub-investigators with any adverse events and updates to patient’s medical history and concomitant medications/procedures
  • Coordinate and oversee patient visits remotely and on-site for clinical trials of RSV, COVID-19, Influenza, Epstein-Barr Virus, Herpes-Zoster, Gout and Asthma.
  • Create and maintain a safe and comfortable environment for all clients
  • Guide clients through the neurofeedback process, including equipment fitting and an explanation of the session, answering any questions as necessary
  • Communicate with clinical team effectively and routinely regarding patient data to promote positive patient outcomes
  • Sanitize and clean training stations and equipment after each session
  • Identify behaviors requiring intervention and obtain assistance from clinicians to complete intervention
  • Document observations and baseline measurements in medical record

Medical Assistant

06.2014 - 03.2019
  • Proficiently practice taking vitals and patient history, including but not limited to, blood pressure, EKG, medication list, family and medical histories
  • Initiate patient visits and efficiently pace physicians’ schedules; smoothly conducting up to 30 patient visits daily along with various tests and procedures
  • Regulate and adapt to evolving hospital protocols and general workflow of the office
  • Maintain a clear and accurate electronic medical record with strong attention to detail
  • Respond to emergent situations in office and triage calls in an effective, yet compassionate manner

Education

Bachelor of Medicine, Bachelor of Surgery -

Hebei Medical University
03.2011

Skills

  • Good clinical practices
  • Electronic data capture
  • Documentation management
  • Informed consent
  • Data Collection
  • Patient monitoring
  • Patient Recruitment
  • Managing and coordinating all aspects of a clinical trial,ensuring smooth execution and adherence to protocols and regulations
  • communicate with participants investigators and sponsors

Certification

  • Certificate in Understanding Dementia, University of Tasmania, AU - 2014
  • Certified Medical Assistant 2021
  • Certificate in Biomedical Research
  • OSHA Bloodborne Pathogens
  • Shipping and Transport of Regulated Biological Materials
  • GCP for Clinical Trials with Investigational Drugs and Medical Devices (U.S. FDA Focus)

LANGUAGES

English, Hindi, Punjabi and Urdu

Timeline

Clinical Research Coordinator

05.2023 - 05.2025

Medical Assistant

06.2014 - 03.2019

Bachelor of Medicine, Bachelor of Surgery -

Hebei Medical University

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