Remote Clinical Project Manager: Lead Life-Saving Trials

Clario; Northern (KY); Hybrid; USD 110,000 - 160,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

Paid time off

Remote/hybrid work options

Tuition reimbursement

EAP & wellness programs

Life insurance

Disability insurance

Job summary

Clario is seeking a Clinical Project Manager to lead cross-functional clinical projects from start-up through closeout. You will drive study plans, timelines, budgets, and stakeholder communications in a fast-paced environment.

The role emphasizes strong leadership, regulatory knowledge, and collaboration with sponsors, sites, and internal teams to deliver high-quality data solutions for clinical research.

Qualifications

• Bachelor's degree in Life Sciences, Pharmacy, Nursing, Healthcare, or related field (or equivalent).
• Experience managing clinical research projects with investigational products in CRO/pharma settings.
• Knowledge of GCP, ICH guidelines, and FDA regulations.

Responsibilities

• Lead study start-up activities by reviewing protocol requirements, developing project plans, defining timelines and milestones.
• Establish and maintain project communication plans and stakeholder updates for sponsors and leadership.
• Identify project success metrics, oversee progress, and manage risks and resources.
• Manage project finances including forecasting, billing, and revenue reporting.
• Ensure compliance with SOPs, regulatory requirements, and quality standards.
• Coordinate data collection across sites and support successful delivery.

Skills

Project management

Stakeholder management

GCP/ICH knowledge

Microsoft Office

Clinical trial experience

Education

Bachelor's degree in Life Sciences or related field

Tools

MS Project

CTMS familiarity

Job description

Clario is seeking a Clinical Project Manager to lead cross-functional clinical projects from start-up through closeout. You will drive study plans, timelines, budgets, and stakeholder communications in a fast-paced environment.

The role emphasizes strong leadership, regulatory knowledge, and collaboration with sponsors, sites, and internal teams to deliver high-quality data solutions for clinical research.