
Start-up Manager, FSP
Posted 3 days ago

Posted 3 days ago
This is a fully remote position, open to applicants in Brazil.
• Oversee intricate site operations while ensuring adherence to regulatory requirements.
• Assist with site recruitment and training initiatives.
• Promote collaboration between trial sites and internal teams.
• Coordinate the delivery of site activation within assigned projects in a matrix environment.
• Supervise site activation in accordance with project timelines and quality benchmarks.
• Manage the flow of information among PPD teams, clients, and functional departments.
• Create suggested project implementation plans and guidelines utilizing PPD tools.
• Monitor and assess project status, providing metrics to senior management.
• Recognize risks and formulate contingency strategies.
• Oversee the financial and contractual aspects of studies related to site activation.
• Establish controls to ensure project resources and expenses align with budgets.
• Manage the technical and operational facets of site activation, including feasibility, site contracts, and country teams.
• Oversee the assigned scope of work in relation to timelines, costs, and quality standards.
• Identify and analyze issues that may impact successful site activation.
• Interpret complex data, make informed business decisions, and ensure effective solution implementation.
• Cultivate customer relationships in accordance with assigned projects.
• Bachelor's degree or equivalent formal academic/vocational qualification.
• A minimum of 5 years of relevant prior experience.
• Consideration may be given for equivalency through a combination of relevant education, training, and/or direct experience.
• Proven ability to work effectively within cross-functional teams.
• Understanding of cross-functional project management principles.
• Strong organizational and multitasking abilities.
• Keen attention to detail.
• Capability to identify and address risks associated with contractual obligations.
• Cross-cultural awareness and adaptability.
• In-depth understanding of clinical research/development, medical and therapeutic areas, study phases, and medical terminology.
• Ability to lead, interact with, and coordinate cross-functional project teams.
• Comprehensive knowledge of clinical development guidelines and directives.
• Proficient in using both in-house and commercially available software.
• Effective communication and listening skills.
• Capacity to perform well under pressure and multitask.
• Consistent and regular attendance.
• Ability to maintain an upright and/or stationary position for 6–8 hours daily.
• Capability for frequent mobility, occasional crouching and stooping, and frequent bending and twisting.
• Ability to lift and carry weights of 15–20 lbs.
• Willingness and ability to travel up to 20% domestically and internationally.
• Capability to work in office/laboratory and clinical settings, with potential exposure to biological fluids, infectious organisms, and electrical office equipment.
• Ability to use necessary personal protective equipment, including protective eyewear, garments, and gloves.
• Fully remote work arrangement.
• Standard Monday–Friday work hours.
• Opportunities for collaboration and professional development.
• Global team environment.
• Occasional travel opportunities to both domestic and international site locations.
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