Remotely
gcpdata qualityclinical researchregulatory compliancesite managementrisk assessmentmonitoringich guidelines
Job Description
📋 Description
- Act as primary Sponsor point of contact for investigative sites
- Provide contextual information on clinical trials to stakeholders and strengthen AbbVie positioning
- Train and motivate site staff and principal investigator on clinical trial goals and protocol
- Conduct site evaluation, training, routine monitoring (onsite/offsite), and site closure activities
- Ensure compliance with protocol, monitoring plans, regulations, GCP, ICH guidelines, AbbVie SOPs
- Customize site engagement strategy, gather insights, and track progress/impact
🎯 Requirements
- Bachelor's degree or equivalent degree; health related preferred (e.g., Medical, Scientific
- Valid driver's license
- Minimum of 1 year of clinically related experience, of which 6 months in clinical research
- Knowledge of therapeutic area indications with ability to understand and apply scientific concepts
- Advanced knowledge of local regulatory and legal requirements, ICH/GCP Guidelines and applicable
- Demonstrate strong cross-functional collaboration skills
🎁 Benefits
- Life assurance
- Medical plan
- Flexible benefits
- Company car
- Comprehensive package (additional details during recruitment process)
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