Instagram
youtube
Facebook

Clinical Research Coordinator

3+ years
Not Disclosed
10 Jan. 31, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

๐Ÿ“Œ Clinical Research Coordinator – Bengaluru, India | IQVIA

๐Ÿ’ผ Company: IQVIA
๐Ÿ“ Location: Bengaluru, India
๐Ÿ•’ Type: Full-time
๐Ÿ“Œ Job ID: R1463146

About IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. We accelerate the development and commercialization of medical treatments to improve patient outcomes and global health.

Position Overview

The Clinical Research Coordinator (CRC) will perform various clinical procedures to collect, record, report, and interpret data on patients enrolled in clinical studies. The role requires compliance with study protocols, Good Clinical Practice (GCP), and Standard Operating Procedures (SOPs).

Key Responsibilities

โœ” Clinical Research Support: Assist investigators in preparing and executing clinical studies, review study protocols, Case Report Forms (CRFs), and electronic data capture systems.
โœ” Recruitment and Screening: Recruit and screen patients for clinical trials and maintain screening logs.
โœ” Regulatory Documentation: Submit regulatory/ethics documentation as required by FDA and other regulatory bodies.
โœ” Study Visits: Schedule and execute study visits and perform study procedures.
โœ” Data Collection: Collect, record, and maintain research subject study data per protocol, ensuring accuracy and completeness.
โœ” Lab Testing: Handle lab testing, specimen collection tubes, and lab logistics.
โœ” Safety Monitoring: Monitor subject safety and report adverse reactions.
โœ” Team Collaboration: Participate in study “huddles” and assist in quality checking and query resolution.
โœ” Complex Procedures: Perform procedures like ECG, spirometry, vital signs, dose verification, and cardiac telemetry monitoring.
โœ” Training and Auditing: Train new staff and assist with adherence to training requirements and audits.
โœ” Study Visits: Attend study monitoring visits, audits, and regulatory inspections.

Qualifications

๐ŸŽ“ Education:

  • Bachelor's degree or High School Diploma (with additional experience).

๐Ÿ’ผ Experience:

  • Minimum of 3 years in a clinical environment or related medical setting (e.g., medical assistant, laboratory technician).
  • Strong knowledge of clinical trials and GCP principles.
  • Proficiency in MS Windows and Office applications.

๐Ÿ”‘ Skills:

  • Ability to perform clinical procedures such as intravenous catheter insertion and spirometry.
  • Strong attention to detail and interpersonal skills.
  • Ability to work effectively with colleagues, managers, and clients.

Apply Now