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 site qualification, initiation, interim monitoring, and study closeout visits for Phase 1-4 studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs).
- Overviews the overall activities of site personnel over whom there is no direct authority and motivates/influences them to meet study objectives.
Proactively manages the site and ensures action plans are put into place as needed to ensure compliance.
Ensures regulatory inspection readiness at assigned clinical sites.
- Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
- Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members.
- Manages investigator payments as per executed contract obligations.
Negotiates investigator/hospital agreements with stakeholders.
Maintains and completes own expense reports as per local and applicable guidelines.
- Identifies, evaluates, and recommends new/potential investigators/sites on an ongoing basis.
Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.
Minimum Requirements: - Appropriate tertiary qualification, health-related (e.G., Medical, Scientific, Nursing) preferred.
- Minimum of 2 years of independent clinical research monitoring.
Experience in on-site monitoring of investigational drug or device trials is required.
- Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials.
- Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines, and applicable regulations.
- Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines.
- Strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity.
- Ability to address study-related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated.
- Ability to use functional expertise and exercise good judgment.
- Demonstrated business ethics and integrity.
- High English level is required as well as Spanish.
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