
Start-up Manager
Posted 3 days ago

Posted 3 days ago
This is a fully remote position, open to applicants in North Carolina.
• Collaborate with colleagues in a matrix structure to ensure site activation for designated projects.
• Supervise site activation in accordance with established timelines and quality benchmarks.
• Facilitate the flow of information between PPD teams, clients, and various functional departments.
• Create project implementation strategies and guidelines utilizing PPD tools.
• Track and assess project progress and provide metrics to senior management.
• Identify potential risks and formulate contingency plans.
• Oversee financial and contractual elements of studies related to site activation.
• Set up controls to ensure project resources and expenses are aligned with budgets.
• Manage the technical and operational facets of site activation, including feasibility studies, site contracts, and coordination with country teams.
• Oversee the assigned scope of work regarding timelines, costs, and quality standards.
• Recognize and assess issues that may impact the success of site activation and implement effective solutions.
• Cultivate customer relationships in line with assigned projects.
• Travel to domestic and international site locations up to 20% of the time.
• A Bachelor's degree or equivalent relevant academic/vocational qualification.
• Prior experience of at least 5 years in a similar role.
• Consideration may be given to a combination of suitable education, training, and/or directly related experience.
• Proficient in collaborating effectively with cross-functional teams.
• Familiarity with cross-functional project management principles.
• Strong organizational and multitasking abilities.
• Keen attention to detail.
• Capability to identify and address risks associated with contractual obligations.
• Awareness and adaptability to cross-cultural environments.
• In-depth understanding of clinical research, development, medical and therapeutic areas, study phases, and medical terminology.
• Ability to lead, communicate, and coordinate with cross-functional project teams.
• Extensive knowledge of clinical development guidelines and directives.
• Proficient in using both in-house and commercially available software.
• Strong verbal and written communication skills.
• Ability to perform under pressure and manage multiple tasks simultaneously.
• Consistent and reliable attendance.
• Join a global team environment.
• Opportunities for collaboration and professional development.
• Work in a setting focused on scientific excellence.
• Occasional travel opportunities to domestic and international site locations.
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