Lead Study Monitor Europe

Clinglobal Group; Milano; Remoto; EUR 45.000 - 65.000; Tempo pieno

Descrizione del lavoro

A leading company in the Animal Health Contract Research sector seeks a senior Study Monitor to oversee clinical trials. This remote role involves leading teams across Europe, ensuring adherence to study protocols, and managing site relationships. The ideal candidate will have a Bachelor's degree in Life Sciences and at least five years of relevant experience.

Competenze

• Minimum of five years' experience in Study Monitoring within Animal Health or Human Pharma sectors.
• Familiarity with FDA/CVM, EMA, VMD, VICH Guidelines.
• Proficiency in one or more other European languages is advantageous.

Mansioni

• Lead and coordinate a team of study Monitors across multiple countries.
• Monitor study sites and verify data collection.
• Compile Monitor reports and assist with site evaluations.

Conoscenze

Strong technical writing

Oral presentation skills

Project management capabilities

Organizational skills

Formazione

Bachelor's degree in a relevant Life Sciences field

Strumenti

Electronic Data Capture Systems

Descrizione del lavoro

Clinglobal is part of a group of Animal Health Contract Research Organisations servicing the global animal health industry.

We're actively seeking a Europe-based senior Study Monitor to join our expanding Field Clinical Trials team This role provides the flexibility to work remotely, with occasional visits rto Clinglobal group’s offices.

• Primary Job Purpose

Lead the Monitor team across all participating countries in a specific study and actively engage in Monitoring activities. Collaborate with Study Monitors and support the Clinical Trial Project Manager to ensure studies adhere to scientific design and timelines outlined in the study Protocol, Standard Operating Procedures (SOPs), Policies, regulatory guidelines, and quality standards (e.g., VICH GL9 GCP).

Serve as the primary contact for Study Monitors and their designated clinical study sites / Investigators, providing consistent updates to the Clinical Project Manager.

• Job Specific Duties and Responsibilities
• Coordinate and lead a team of study Monitors working on a particular study.
• Monitor study sites, including activities associated with study initiation, execution, close-out, and submission, and verify the data collected.
• Train sites on study protocols and GCP.
• Compile Monitor reports to report on the progress of the study and obtain corrective actions as necessary.
• Assist with site selection and evaluation.
• Serve as point of contact between the Clinglobal group and study sites / Investigators.
• Mentor and train fellow team members on study Monitor management.
• Assist the Clinical Trial Project Manager with study activities, including but not limited to reviewing draft protocols, overseeing sites’ budgets and invoices, and maintenance of monitoring tools.
• Serve as point of contact for new clinical study sites / Investigators.
• Provide oversight of study master files (electronic and paper) and prepare the study files for archiving / submission.
• Liaise and coordinate with different departments, partner companies, and external partners to support the Clinical Trial Project Manager in ensuring that necessary resources are available to perform the required function at the planned time to achieve the project outcomes.
• Ensure study sites / Investigators fulfil their responsibilities to meet the agreed timelines, quality, and cost.
• Proactively identify risks that might jeopardize projects, e.g., technical feasibility, sites’ suitability, timely execution, budget constraints, etc.
• Develop and maintain project management tools, including but not limited to Gantt charts, project budgets, forecasts, etc.
• Promote the organization’s capabilities and values internally and externally.
• Leading global study-level documentation and required tool and systems set-up.
• Author and review monitoring-related controlled documents, where applicable.
• Qualification, Training and Experience Requirements
• Bachelor's degree in a relevant Life Sciences field.
• Minimum of five years' experience in Study Monitoring within Animal Health or Human Pharma sectors.
• Industry knowledge, including familiarity with FDA / CVM, EMA, VMD, VICH Guidelines, Clinical Field Trials, and Data quality requirements.
• Strong technical writing and oral presentation skills in English; proficiency in one or more other European languages is advantageous.
• Competence in Electronic Data Capture Systems.
• Demonstrated exceptional organizational and project management capabilities.
• Important Note to Applicants

This is a remote position with potential for regular travel.

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