About the job
The Senior Clinical Research Associate at AbbVie plays a crucial role in advancing life-changing therapies by overseeing and monitoring clinical trial sites. This job is all about ensuring the highest standards of quality, compliance, and patient safety while collaborating with a dedicated team. AbbVie values a supportive and inclusive work environment, where every team member contributes to making a remarkable impact on patients' lives.
You'll be responsible for
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Overseeing clinical trial sites
Acting as the primary Sponsor point of contact for investigative sites, ensuring compliance with clinical trial protocols and regulations.📚
Training site staff
Aligning, training, and motivating site staff and principal investigators on clinical trial goals and patient treatment principles.📊
Monitoring study performance
Conducting routine monitoring and risk assessments to ensure patient safety and effective study execution.Key criteria
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Clinical research monitoring experience
3+ years of experience in clinical research monitoring.View
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ICH/GCP guidelines knowledge
Proven understanding of ICH and GCP guidelines.View
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Cross-functional collaboration skills
Demonstrated ability to collaborate with diverse stakeholders.View
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