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Clinical Project Manager Group Lead

Reference:ARNW-161818
Location: Dublin
Qualification:Degree
Experience:10+ Years
Job Type:Permanent
Salary:Not Disclosed
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Clinical Project Manager Group Lead
Our client, a multinational pharmaceutical role are currently recruiting for a Clinical Project Manager Group Lead to join their team on a permanent basis. This is a newly created role due to the growth of the business.

Responsibilities
• Lead and develop the Clinical Project Management team in Ireland to ensure staffing, training and development
• Create & develop local processes to implement the End to End Clinical Trial Service strategy – collaboration with counter-parts globally is essential
• Provide sound leadership and superior decision-making support as well as services’ experience and process excellence to drive quality service implementation, cost optimization and continuous improvement
• Build on existing processes or develop new processes to provide guidance to the clinical trial teams to ensure that industry best-practice standards in operational and performance excellence are met and customer expectations are met or exceeded.
• Drive improvement in performance of service quality, turnaround time, customer feedback and other key performance measures and benchmark against best-in-class
• Establish robust relationships with other Operations teams, understanding the needs of stakeholders to identify potential service opportunities or improvements in service processes
• Provide clinical operational input to activities related to planning, execution and reporting of clinical trials to support clinical trial management
• Proactively identify areas of potential concern, initiating corrective action when necessary, and identify innovative ways to improve productivity. Function as escalation contact point for trial teams
• Ongoing review of clinical trial data in collaboration with appropriate members and Brand Safety Leader, as needed
• Champion cross-functional interaction and collaboration to ensure quality delivery of studies
• In collaboration with QA, manage audits and regulatory inspections and create an audit readiness working environment
• Interact with sourcing department to ensure selection of optimal vendors essential to service delivery and continual optimization of vendor services

Requirements
• Degree or PhD in Life sciences/Pharmacy, with strong knowledge of clinical development and trial execution
• 10 years of clinical research experience, including clinical trial management experience, with solid knowledge of global drug development process
• 4 years of people management experience required, this may include people management in a matrix environment (Responsibility for 5 to 10 direct reports, depending on new trials & programs. Responsible for oversight of provision of Clinical Trials services)
• Excellent understanding of clinical trial methodology, GCP and medical terminology
• Advanced planning and tracking skills with attention to detail. Well-organized, excellent time management with respect to priorities and self-management
• Strong management, interpersonal, communication, and problem-solving skills
• Quick action taker. Involves the right team members in the right situation at the right time
• Ability to mentor, coach associates, and to coordinate interactions with internal and external partners
• Superior people management skills with demonstrated positive leadership, innovative, and

If you would like further Information you can contact the recruiter directly:

Sinead Cullen | Tel: +353 (0) 1 507 9252




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