Job Title: Clinical Pharmacology & Pharmacometrics (CPP) Project Coordinator
Location: Titusville, NJ (Hybrid)
Contract Length: 06+ months
Pay Range: $35/hr. - $37.05/hr.
Position Summary:
The CPP Project Coordinator provides administrative, project coordination, process, and operational support to enable effective execution of priorities across Clinical Pharmacology & Pharmacometrics (CPP). The role serves as a central point of coordination for the CPP Leadership Team and is responsible for supporting meeting and event coordination, leadership support activities, operational reporting, tracker maintenance, communications, and follow-up on key business activities.
This position requires a highly organized, proactive, and collaborative individual who can work independently, manage competing priorities, and support a global, matrixed environment. The successful candidate will communicate effectively across functions and levels, demonstrate sound judgment and attention to detail, and help ensure smooth day-to-day operations and business continuity.
The individual must be able to anticipate needs, identify potential issues, coordinate actions across stakeholders, and ensure timely follow-through. This role also requires a positive, adaptable mindset, a willingness to embrace new ways of working, strong learning agility, and the ability to leverage AI-enabled technologies and other digital solutions to enhance efficiency and support continuous improvement.
Principal Responsibilities:
" Provide approximately 60% executive and administrative support to CPP Leadership, including strategic global calendar management, meeting coordination, stakeholder support, travel support, and timely follow-up.
" Maintain complex, changeable global calendars across time zones while accommodating multiple stakeholder requirements with professionalism, discretion, and sound judgment.
" Provide approximately 40% project, process, and business operations support across CPP priorities, including coordination, tracking, reporting, follow-up, process improvement, and operational execution.
" Maintain and enhance CPP operational reporting tools, trackers, dashboards, and data sources to support leadership reviews, resource planning, financial oversight, and informed business decision-making.
" Work independently once trained by taking clear notes, referencing available materials, applying prior learning, and following through on commitments.
" Proactively anticipate needs, identify gaps or risks, and recommend practical solutions while knowing when review, escalation, or alignment is required.
" Build productive relationships and collaborate effectively with CPP colleagues, leaders, business partners, and external vendors, including when priorities or working styles differ.
" Support administrative and operational activities such as meeting logistics, communications, knowledge management, and resource tracking.
" Navigate business tools and systems, including the ability to locate, interpret, and summarize information from dashboards or reports.
" Use AI-enabled platforms, such as Client Copilot, Claude, or similar tools, to improve efficiency, streamline workflows, support drafting or summarization, and identify process improvement opportunities.
" Demonstrate strong organization, time management, attention to detail, and ability to manage multiple priorities in a dynamic global environment.
Principal Relationships
" Primary reporting structure: Reports to CPP Business Operations Lead.
" Primary interfaces: CPP Business Operations Lead, Vice President of CPP, CPP Project Coordinators and Administrative Assistants, CPP leadership and staff.
" External interfaces: Contracted partners, consultants, suppliers, and vendors, as applicable.
Education and Experience Requirements:
" Associates degree or equivalent experience and 5 years of relevant work experience is preferred; experience in pharmaceutical or biotech research and development is a plus.
" Proven experience and practical knowledge in executive administrative support, project coordination, and project management with matrixed responsibilities in the pharmaceutical industry is required.
" Experience supporting senior leaders or executives, including complex calendar management across global time zones, is strongly preferred.
" Experience working in a global or matrixed organization, including supporting stakeholders across time zones, is strongly preferred.
" High proficiency in MS Office Suite, including Word, Excel, PowerPoint, and Outlook.
" Proven experience using AI-enabled platforms, such as Client Copilot, Claude, or similar tools, to create efficiencies, improve ways of working, and support productivity.
" Strong written, verbal, presentation, and interpersonal communication skills, with the ability to interact professionally across functions and levels.
" Demonstrated ability to work independently, stay organized, manage time effectively, and follow through on deliverables.
" Positive, flexible, and collaborative mindset with a willingness to adapt, work well with others, and contribute to continuous improvement.
" Flexibility in working hours is occasionally required to effectively support global teams.
" Demonstrated experience supporting projects and/or business operations in a matrixed environment.
" Ability to travel to Spring House, PA maybe once a month, if needed only
Preferred Attributes:
" Proactive, resourceful, and able to anticipate what is needed and take appropriate action.
" Organized and disciplined in managing information, notes, deadlines, calendars, and follow-ups.
" Comfortable asking thoughtful questions when clarification is needed while using available training, documentation, and prior guidance.
" Open to feedback and able to incorporate review comments into improved work products.
" Able to balance independence with appropriate escalation, review, and alignment.
" Professional presence and confidence when interacting with cross-functional stakeholders and senior leaders.
" Collaborative, respectful, and positive team member who remains flexible during change.