
Start-up Manager
Posted Oct 30

Posted Oct 30
This is a fully remote position, open to applicants in Mexico.
• Oversee intricate site operations while ensuring adherence to regulatory standards.
• Assist with site recruitment and training initiatives.
• Promote teamwork between trial sites and internal departments.
• Work in conjunction with matrixed team members to achieve site activation for designated projects.
• Supervise site activation in accordance with established timelines and quality benchmarks.
• Manage the flow of information among PPD teams, clients, and functional areas.
• Create project implementation strategies and guidelines utilizing PPD tools.
• Track and assess project progress and deliver metrics to senior management.
• Recognize potential risks and formulate contingency plans.
• Handle financial and contractual elements of studies pertaining to site activation.
• Set up controls to align project resources and expenditures with budgetary limits.
• Oversee the technical and operational components of site activation, including feasibility assessments, site contracts, and coordination with country teams.
• Manage the designated scope of work in relation to timelines, costs, and quality standards.
• Identify and assess challenges that may impact successful site activation and implement corrective measures.
• Foster client relationships that are in line with assigned projects.
• Bachelor's degree or an equivalent formal academic/vocational qualification.
• Minimum of 5 years of relevant experience.
• Equivalency may include a blend of appropriate education, training, and/or directly related experience.
• Proven ability to work effectively with cross-functional teams.
• Familiarity with cross-functional project management principles.
• Strong organizational and multitasking capabilities.
• Keen attention to detail.
• Capacity to identify and address risks related to contractual obligations.
• Cross-cultural sensitivity and adaptability.
• In-depth understanding of clinical research and development, medical and therapeutic fields, study phases, and medical terminology.
• Ability to lead, liaise with, and coordinate cross-functional project teams.
• Comprehensive knowledge of clinical development guidelines and directives.
• Capability to work in office, laboratory, and/or clinical settings.
• Willingness to travel occasionally, up to 20%, including domestic and international site locations.
• Ability to remain upright and/or stationary for 6–8 hours per day.
• Capacity to perform repetitive hand movements and maintain frequent mobility.
• Ability to lift and carry weights of 15–20 lbs.
• Proficient in accessing and utilizing both in-house and commercial computer software.
• Regular and consistent attendance is required.
• Global team environment.
• Opportunities for collaboration and professional development.
• Commitment to scientific excellence.
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