
Start-up Manager, FSP
Posted 3 days ago

Posted 3 days ago
This is a fully remote position, open to applicants in Mexico.
• Oversee intricate site operations while ensuring compliance with regulatory standards.
• Assist in recruitment and training initiatives for the site.
• Promote collaboration among trial sites and internal teams.
• Work within a matrix environment to facilitate site activation for designated projects.
• Supervise site activation in accordance with established timelines and quality benchmarks.
• Manage the flow of information between PPD teams, clients, and various functional departments.
• Create project implementation plans and guidelines utilizing PPD tools.
• Track and assess project status, providing metrics to upper management.
• Recognize risks and formulate contingency plans.
• Handle financial and contractual elements of studies related to site activation.
• Implement controls to ensure project resources and expenses align with budgets.
• Oversee the technical and operational dimensions of site activation, including feasibility, site contracts, and country teams.
• Manage the assigned scope of work concerning timelines, costs, and quality standards.
• Identify and analyze challenges affecting successful site activation and execute solutions.
• Cultivate customer relationships pertinent to assigned projects.
• A Bachelor's degree or an equivalent relevant formal academic or vocational qualification.
• Prior experience of at least 5 years in a similar role.
• A suitable combination of education, training, and/or directly related experience may be accepted.
• Proficiency in collaborating effectively with cross-functional teams.
• Familiarity with cross-functional project management principles.
• Strong organizational and multitasking capabilities.
• Meticulous attention to detail.
• Ability to identify and address risks associated with contractual obligations.
• Cross-cultural sensitivity and adaptability.
• Knowledge of clinical research/development, medical and therapeutic fields, study phases, and medical terminology.
• Capability to lead, communicate with, and coordinate cross-functional project teams.
• Understanding of clinical development guidelines and directives.
• Proficient in accessing and utilizing computer software.
• Strong verbal communication skills and comprehension of spoken information.
• Capacity to perform under pressure and manage multiple tasks.
• Consistent and regular attendance is required.
• Ability to work in an office, laboratory, and/or clinical setting.
• Competence in using personal protective equipment such as eyewear, garments, and gloves.
• Ability to remain upright and/or stationary for 6 to 8 hours daily.
• Capability to perform repetitive hand movements.
• Frequent mobility is necessary; occasional bending, stooping, crouching, and twisting may be required.
• Ability to lift and carry weights of 15 to 20 lbs.
• A global team environment.
• Opportunities for collaboration and professional development.
• Occasional travel to both domestic and international site locations.
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