North AmericaFull TimeOther
Remotely
gcpclinical researchregulatory compliancedata integritysite managementmonitoringall otherichtrial execution
Job Description
📋 Description
- Advance AbbVie\'s pipeline by striving for excellence in clinical research and partner with study
- Focus on site clinical research to ensure proper trial conduct, data integrity, and study
- Lead and mentor monitoring teams; align site staff and investigators with trial goals and patient
- Conduct site evaluations, training, monitoring activities, and site closure with adherence to
- Develop and optimize site engagement strategies and recruitment/retention plans based on patient
🎯 Requirements
- Appropriate tertiary qualification in health-related disciplines preferred.
- Minimum 3 years of clinically related experience, with 2 years in independent clinical research
- Knowledge of regulatory requirements (ICH/GCP) and risk-based monitoring; strong communication and
- Excellent planning, organizational, and stakeholder engagement abilities; ability to work in
- Advanced ability to leverage technology/tools to provide site-centric support.
- Ability to mentor junior CRAs and contribute to onboarding and training.
🎁 Benefits
- Professional development
- Paid time off, wellness programs, retirement savings
- Competitive compensation
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