**Company Description**
Describe the primary goals, objectives or functions or outputs of this position.
To enable AbbVie’ s emergence as a world class R&D organization, the position anticipates and proactively solves studyrelated clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol level execution of SMM deliverables involving start-up, execution, and close-out of studies.
Responsibilities:
List up to 10 main responsibilities for the job. Include information about the accountability and scope.
- Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research.
- Conducts s...