Clinical Research Coordinator

IQVIA

Bangalore, India
Clinical research support
Good clinical practice (gcp)
Clinical procedures execution
Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled in clinical studies according to protocol and regulatory standards

Job Summary

  • Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled in clinical studies according to protocol and regulatory standards.
  • Assist investigator in ensuring research study objectives are met on time, within budget, and according to applicable protocol requirements and quality standards.
  • Prepare for and attend study monitoring visits, audits, and regulatory inspections with clinical research regulatory agencies.

Matching Summary

Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled in clinical studies according to protocol and regulatory standards.

Skills & Requirements

Must-have

  • clinical research support
  • Good Clinical Practice (GCP)
  • clinical procedures execution
  • regulatory and ethics documentation
  • patient recruitment and screening
  • data quality checking and query resolution

Nice-to-have

  • excellent interpersonal skills
  • attention to detail
  • effective working relationships
  • training and mentoring site staff

Key Requirements

  • Bachelor's Degree or High School Diploma
  • 3 years relevant clinical experience
  • applicable certifications and licenses
  • working knowledge of clinical trials
  • knowledge of Good Clinical Practices (GCP)

Work Rights

Not specified

Tailored Resume

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