
Clinical Project Research Manager – Central Site
Posted 6 days ago

Posted 6 days ago
This is a fully remote position, open to applicants in United States.
• Lead project teams at UBC to achieve project milestones at the site level.
• Oversee all facets of project execution from initiation to conclusion from a site perspective.
• Implement operational components of assigned project activities and special initiatives.
• Manage projects in accordance with the defined scope of work and within the agreed budget.
• Handle revenue and invoicing for projects at the central site.
• Create plans and procedures to meet contracted milestones.
• Monitor the progress of projects against set plans and ensure adherence to compliance standards.
• Develop project timelines and coordinate the creation of deliverables.
• Prepare agendas for project meetings and compile minutes and action logs.
• Track project budgets in relation to contract milestones.
• Act as UBC’s primary liaison with the sponsor for the central site and escalate concerns for the central site team.
• Organize and facilitate meetings for the central site.
• Ensure that project training is conducted and assist with training as assigned.
• Present project information during bid defenses, client meetings, and UBC's monthly project review meetings.
• Maintain project documentation to ensure readiness for audits.
• Participate in sponsor/regulatory audits as needed.
• Assist in leading process improvement initiatives.
• Establish, implement, and track key metrics to report on project and initiative progress.
• Coordinate and ensure the upkeep of the Electronic Investigator Site File.
• Supervise Study Coordinators and Senior Study Coordinators.
• Bachelor’s degree or equivalent professional experience.
• Experience in Clinical Project Management at a research or academic site.
• Previous experience in people management or relevant leadership roles.
• Strong written, verbal, and interpersonal communication skills.
• Demonstrated supervisory and team leadership abilities.
• Excellent stakeholder management and relationship-building capabilities.
• Strong presentation and facilitation expertise.
• Ability to independently evaluate issues, mitigate risks, and make informed decisions using critical judgment.
• Solution-oriented mindset with a proactive approach to problem-solving.
• Comprehensive understanding of regulatory requirements, including Good Clinical Practice (GCP), ICH guidelines, and related regulations.
• Willingness to travel up to 10% as required by the position.
• Remote work opportunities.
• Competitive salary packages.
• Opportunities for professional growth and promotion.
• 401K plan with company match.
• Tuition reimbursement program.
• Flexible work environment.
• Discretionary Paid Time Off (PTO).
• Paid holidays.
• Employee assistance programs.
• Medical, dental, and vision coverage.
• Health Savings Account (HSA) / Flexible Spending Account (FSA).
• Access to telemedicine services (virtual doctor appointments).
• Wellness programs.
• Adoption assistance.
• Short-term disability coverage.
• Long-term disability coverage.
• Life insurance.
• Discount programs.
Mercor
ICF
ICF
The Cigna Group
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