
Start-up Manager, FSP
Posted Oct 30

Posted Oct 30
This is a fully remote position, open to applicants in Brazil.
• Oversee intricate site operations while ensuring adherence to regulatory standards.
• Assist in recruitment and training initiatives at the site level.
• Promote cooperation between trial sites and internal teams.
• Work in conjunction with matrixed team members to facilitate site activation for designated projects.
• Supervise site activation in accordance with established timelines and quality benchmarks.
• Coordinate the flow of information among PPD teams, clients, and functional departments.
• Create project implementation plans and guidelines utilizing PPD tools.
• Monitor and assess project status, completion, and metrics for upper management reporting.
• Identify potential risks and develop contingency plans.
• Handle financial and contractual elements associated with site activation.
• Establish controls to ensure alignment of project resources and expenditures with budgets.
• Manage the technical and operational components of site activation, which include feasibility studies, site contracts, and coordination with country teams.
• Oversee the assigned scope of work in relation to timelines, costs, and quality standards.
• Identify and assess fundamental issues related to site activation and implement effective solutions.
• Cultivate customer relationships that correspond with assigned projects.
• Bachelor's degree or equivalent, along with relevant formal academic or vocational qualifications.
• A minimum of 5 years of pertinent experience (or comparable experience, education, training, and/or closely related experience).
• Proficiency in working effectively with cross-functional teams.
• Understanding of cross-functional project management principles.
• Strong organizational and multitasking capabilities.
• Keen attention to detail.
• Ability to identify and address risks associated with contractual deliverables.
• Cultural awareness and adaptability.
• Thorough knowledge of clinical research and development, medical and therapeutic domains, study phases, and medical terminology.
• Capability to lead, engage, and coordinate cross-functional project teams.
• Extensive understanding of clinical development guidelines and directives.
• Proficiency in accessing and utilizing both in-house and off-the-shelf software applications.
• Strong communication skills for understanding and conveying spoken and written information.
• Consistent and regular attendance is required.
• Ability to work in an office, laboratory, and/or clinical setting.
• Willingness to travel domestically and internationally up to 20% of the time.
• Capability to remain upright and/or stationary for 6–8 hours daily.
• Ability to lift and carry weights between 15–20 lbs.
• A global team environment.
• Opportunities for collaboration and professional development.
• A culture that values passion, innovation, and scientific excellence.
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