Global Trials CRA — Mentoring, Growth & Flexible Hours

iqvia

Singapore

Hybrid

SGD 60,000 - 90,000

Full time

3 days ago
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Benefits offered by this job

Mentoring program
Quarterly performance reviews
Structured training
Global project exposure

Job summary

IQVIA is seeking a Senior CRA/CRA in Singapore to plan and execute site initiation, monitoring and close‑out visits across global trials. You will support recruitment planning, ensure protocol training, and maintain regulatory compliance while communicating with diverse stakeholders.

The role offers mentoring, quarterly performance reviews, and a structured development path in a flexible, hybrid work environment with opportunities to work on cutting‑edge in‑house technology and global projects.

Qualifications

  • University degree in scientific discipline or healthcare.
  • Good knowledge of GCP and clinical research regulatory requirements.
  • Excellent command of English and strong organizational skills.

Responsibilities

  • Performing site selection, initiation, monitoring, and close‑out visits, plus maintaining appropriate documentation.
  • Supporting the development of a subject recruitment plan.
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites.
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate.
  • Managing progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.
  • Collaborating with colleagues and customers and maintaining knowledge of regulatory requirements.

Skills

On-site monitoring
GCP knowledge
English proficiency
Communication skills
Time management
Relationship building
Travel flexibility

Education

University degree in scientific discipline or healthcare

Tools

MS Office

Job description

IQVIA is seeking a Senior CRA/CRA in Singapore to plan and execute site initiation, monitoring and close‑out visits across global trials. You will support recruitment planning, ensure protocol training, and maintain regulatory compliance while communicating with diverse stakeholders.

The role offers mentoring, quarterly performance reviews, and a structured development path in a flexible, hybrid work environment with opportunities to work on cutting‑edge in‑house technology and global projects.

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