
Start-up Manager
Posted Nov 3

Posted Nov 3
This is a fully remote position, open to applicants in Argentina.
• Oversee intricate site operations while ensuring adherence to regulatory standards.
• Assist with site recruitment and training initiatives.
• Promote cooperation between trial sites and internal teams.
• Work within a matrix structure to facilitate site activation for designated projects.
• Supervise site activation in alignment with established timelines and quality benchmarks.
• Manage the flow of information among PPD teams, clients, and various functional departments.
• Create project implementation plans and guidelines utilizing PPD resources.
• Track and assess project progress, providing metrics to senior management.
• Recognize risks and formulate contingency plans.
• Oversee financial and contractual matters related to site activation.
• Establish controls to align project resources and expenditures with budgets.
• Handle feasibility assessments, site contracts, and coordination with country teams.
• Manage the defined scope in relation to timelines, costs, and quality standards.
• Identify and analyze issues impacting successful site activation and implement effective solutions.
• Foster customer relationships in line with assigned projects.
• A bachelor's degree or equivalent formal academic/vocational qualification.
• Relevant experience amounting to at least 5 years.
• An equivalent combination of suitable education, training, and/or directly related experience may also be deemed sufficient.
• Capability to work efficiently within cross-functional teams.
• Familiarity with cross-functional project management principles.
• Strong organizational and multitasking abilities.
• Keen attention to detail.
• Proficiency in identifying and addressing risks associated with contractual obligations.
• Cultural awareness and adaptability.
• Comprehension of clinical research/development, medical and therapeutic domains, study phases, and medical terminology.
• Ability to lead, connect, and coordinate cross-functional project teams.
• Understanding of clinical development guidelines and directives.
• Proficient in using both in-house and commercial software applications.
• Effective communication skills for both spoken and written information.
• Consistent and regular attendance is required.
• Capability to work in an upright or stationary position for 6 to 8 hours daily.
• Willingness to undertake occasional travel, including both domestic and international trips.
• A global team environment.
• Opportunities for collaboration and professional development.
• Possibility of occasional travel to site locations (up to 20%).
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