Immunology CRA II: Drive Impactful Clinical Trials

Allergan

Miami (FL)

On-site

USD 65,000 - 95,000

Full time

3 days ago
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Benefits offered by this job

Paid time off
Medical/dental/vision insurance
401(k)

Job summary

AbbVie in the United States is seeking a Clinical Research Monitor to advance our clinical trial programs, ensuring compliant conduct and high data integrity across sites.

You will partner with investigators and site staff, train teams on study goals, monitor site activities per protocol, and drive improvements in patient recruitment and retention.

The role emphasizes risk assessment, collaboration across functions, and adherence to GCP standards to deliver quality outcomes for patients.

Qualifications

  • 1 year of clinical research monitoring or related experience.
  • Familiar with risk-based monitoring approaches and GCP/ICH guidelines.
  • Ability to train and mentor junior CRAs.
  • Strong collaborative and communication skills.
  • Knowledge of local regulatory requirements.

Responsibilities

  • Serve as primary contact for investigative sites.
  • Align, train and motivate site staff on trial goals.
  • Conduct site evaluation, training, monitoring per protocol.
  • Develop site engagement strategies and report progress using CRM.
  • Mentor junior CRAs and participate in task forces.
  • Monitor for risk signals and implement corrective actions.
  • Ensure data quality and safety reporting to sites.
  • Ensure audit and regulatory inspection readiness.

Skills

Cross-functional collaboration
Planning & organization
Site engagement strategies
Strong interpersonal skills
Critical thinking
Regulatory knowledge

Education

Bachelor's degree or higher in health-related field

Tools

CRM tools
SOPs & GCP knowledge

Job description

AbbVie in the United States is seeking a Clinical Research Monitor to advance our clinical trial programs, ensuring compliant conduct and high data integrity across sites.

You will partner with investigators and site staff, train teams on study goals, monitor site activities per protocol, and drive improvements in patient recruitment and retention.

The role emphasizes risk assessment, collaboration across functions, and adherence to GCP standards to deliver quality outcomes for patients.

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