Sr. Clinical Project Manager - Cardiometabolic

Job Requirements

• Minimum 10 years’ experience in clinical trials (pharma and/or CRO), with at least 5 years as Project Manager
• Extensive metabolic continuum study experience including but not limited to obesity, diabetes, MASH, dyslipidaemia, ASCVD, is required
• Proven ability to create strong relationships with small sponsor stakeholders including CEOs
• Multinational study experience
• Strong knowledge of ICH-GCP and relevant regulations

Responsibilities

• Provide leadership of one or more complex metabolic continuum projects in the delivery of services and key milestones to make sure that projects are delivered according to the client expectations and project scope, time schedules and budget
• Develop study-specific documentation in collaboration with compliance and study teams
• Monitor progress against plans, KPIs, and budgets; adjust as needed
• Identify and mitigate risks proactively
• Report progress to sponsors, internal stakeholders, and steering committees
• Act as the day-to-day contact for sponsors and project teams
• Drive process improvements and contribute to departmental growth
• Manage project finances and support proposals and bid defense meetings
• Resolve complex challenges through effective stakeholder engagement
• Participate in and support commercial-team led activities such as project strategy development, proposal development, BDM and client meetings