Senior Manager Trial Capabilities

Senior Manager Trial Capabilities
Our client, a global pharmaceutical organisation are currently recruiting a Senior Manager to join their newly created Clinical Trials Capabilities team. As Senior Manager you will lead the clinical trial capabilities in support of clinical development. This is an exciting opportunity which will allow you to provide leadership, direction and technical support to the Clinical Trial Capabilities Teams focusing on results and driving efficiency to achieve goals and objectives

Responsibilities:
• Accountable for meeting and exceeding goals for clinical trial initiation for development programs
• Ensure site initiation and maintenance activities comply with local/regional requirements, data privacy requirements and quality standards
• Drive and ensure Site Activation strategies are created and delivered
• Manage communications/relationships and serve as the point of contact for the trial capabilities deliverable during site initiation, maintenance, and close out representing progress to business partners
• Prioritise work to meet portfolio needs
• Ensure flexibility of resources across trial capabilities teams and geographies
• Provide expertise in conducting clinical research and keeping up to date with country/regional regulatory requirements
• Develop and manage strategies to improve customer experience
• Ensure inspection readiness through a complete, accurate and readily available Trial Master File
• Build capabilities in the function through the development and improvement of processes, tools and training and partnering with Clinical Information and Process Automation to leverage technology to increase efficiency of clinical trial capabilities and resources
• Enable a culture of continuous improvement to drive efficiency through process improvement, people skills, and shared learning
• Recruit, develop, and retain a scientific and operationally capable workforce skilled and knowledgeable in clinical development
• Effectively manage an agile organization that continuously meets the needs of a changing portfolio

Requirements:
• Bachelor’s degree preferably in a scientific or health related field, five years clinical research experience or relevant experience preferred
• Understanding of the overall clinical development paradigm and the importance of efficient site initiation
• Previous supervisory experience
• Strong leadership skills and ability to influence others and lead across the business
• Project management processes and skills
• Appreciation of / experience in compliance-driven environment
• Ability to learn and comply with financial and legal guidelines and policies (budget and contract)
• Effective communication, negotiation, and problem-solving skills
• Self-management and organizational skills

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

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