Clinical Site Manager (Project Management) - Melbourne
Fantastic Permanent F/T opportunity to work as a Senior Site Manager with Syneos Health in Melbourne based at Global Pharma Office with great culture!
Summary about this job
Pharmaceuticals & Medical Devices
Company: Syneos Health
Location: Melbourne
Work type: Full Time
Salary: n\a
Phone: +61-7-1545-8330
Fax: +61-8-6092-8748
E-mail: n\a
Site: n\a
Detail information about job Clinical Site Manager (Project Management) - Melbourne. Terms and conditions vacancy
Responsibilities:
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Proactively identifies and resolves potential problems at both country/hub level and engages the Medical
Monitor and/or Protocol Manager to assist in the resolution of more complex issues. -
Possesses substantial and in-depth knowledge typically attained through at least a Bachelors degree (or local
equivalent) in a health-related field and or developmental/clinical experience. -
Proactively seeks to enhance communication skills with both internal (Global level) and all relevant external parties and coaches others to do the same.
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Contributes significantly to study team and coaches site staff to enhance site and hub performance.
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Independently makes decisions and takes action within the scope of Senior Site Manager responsibilities and anticipates and proactively solves study site problems/issues as they occur.
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Exhibits a high level of flexibility and sets an example for the department when leading and adapting to changes.
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Serves as a key resource for colleagues, by providing guidance, leading training and mentoring to other team members through a mentoring process using informal and/or formal presentations.
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Proactively identifies and suggests innovative solutions to accomplish objectives while maximizing utilization of
budget and resources. -
Demonstrates strong leadership skills and role model behaviours.
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Insight and working knowledge of other functional/cross functional roles via co-monitoring, job rotation, audit preparation and inspection readiness.
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Instinctively collaborates across organizational, functional and geographic boundaries to achieve departmental
and company goals. -
Takes appropriate and informed business risk and encourages others to do the same.
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Works independently. Leads or supervises departmental/divisional/role special projects, cross functional and geographic groups, task
forces and study feasibilities as requested. In addition to SME (or similar) role. -
Makes innovative suggestions, as appropriate, to management for process or role change to enhance value of
the position. -
Proactively identifies and resolves potential problems at both country/hub level and engages the Medical Monitor and/or Protocol Manager to assist in the resolution of more complex issues.
Requirements:
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Bachelor's degree or RN in a related field or equivalent combination of education, training and experience
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Experience as a Clinical Site Manager or Project/Study Manager at a senior level within the pharmaceutical, CRO &/or trial research environment.
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Experience with aspects of project management.
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Experience in the conduct and management of Investigator sites from start-up to database lock within expectations set by management
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Experience in effective implementation of clinical plans/documents and document preparation.
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Previous experience working in a team environment within a matrix organization.
To apply, please submit your application via SEEK.