Clinical Central Monitor - Global Vendor job in City of London, England

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Job type: Permanent

Discipline: Operations

Location: United Kingdom

This vacancy has now expired. Please see similar roles below...

Proclinical is seeking a Central Monitor Lead with a strong data analytics aptitude. This role is integral to driving customer success and broad adoption of our advanced statistical algorithms for clinical trial data quality. If you thrive in a dynamic, internationally focused, fast-growing, multi-disciplinary company, this position could be an exciting opportunity for you.

Responsibilities:

Guide data analysts in reviewing Central Monitoring Platform outputs and performing initial investigations of identified risks.
Summarize findings and communicate results to clients, ensuring they understand the impact on their data.
Coach clients' Risk Coordinators in the Signal Management process, defining appropriate follow-up actions and ensuring robust documentation.
Support study teams in adopting an approach to clinical trial monitoring that focuses resources on risks with the most potential to impact patient safety and data quality.
Document and share lessons learned during each client engagement to facilitate cross-study and cross-organization learning.
Participate in the continuous improvement and development of our product solutions and operational processes.

Key Skills and Requirements:

Working knowledge of clinical development process, including study phases and the principles of study design and study execution.
Previous experience with and understanding of clinical trials and clinical data across multiple therapeutic areas.
Previous experience within clinical operations and understanding of key processes including monitoring, data management, (medical) data review and related processes.
Aptitude for data analytics and critical thinking skills to determine the signs of risk.
High degree of accuracy and attention to detail.
Effective English verbal and written communication skills in relating to people both inside and outside the organization in a team environment.
Works independently, ability to multi-task and provide expertise on multiple projects concurrently.
Ability to thrive in a fast-moving environment, under time and resource constraints.

Qualifications Required:

Bachelor's degree or above in a scientific or business-related discipline required.
Proven history within the clinical research industry.
Proven working experience in RBQM/Central Monitoring.
Previous experience as clinical research associate is an advantage.

For more information, please apply today or contact Jack O'Neill on j.oneill@proclinical.com.

Apply Now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.