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Clinical Program Manager at Axle | JobMatcher
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Posted July 21, 2026 About the role Responsibilities Coordinate operational activities for clinical studies and oversee assigned portfolios. Facilitate feasibility assessments, startup activities, and site coordination for multi-center trials. Monitor enrollment and study progress; track milestones and deliverables; report to leadership. Develop and maintain project management plans; monitor schedules, dependencies, and risk mitigation. Home / Jobs / Clinical Program Manager Axle
Posted July 21, 2026 About the role Responsibilities Coordinate operational activities for clinical studies and oversee assigned portfolios. Facilitate feasibility assessments, startup activities, and site coordination for multi-center trials. Monitor enrollment and study progress; track milestones and deliverables; report to leadership. Develop and maintain project management plans; monitor schedules, dependencies, and risk mitigation. JobMatcher Upload your resume once — get matched with real jobs in under a minute.
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© 2026 JobMatcher. All rights reserved.
Oversee regulatory compliance including IRB submissions, regulatory submissions, audits, and inspections.
Coordinate cross-functional communication among investigators, data managers, regulatory staff, and clinical teams; support governance and decision-making. Requirements Master's degree required; relevant certifications preferred (SOCRA, FAC-P/M, FAC-COR, PMP). Experience with clinical trial management systems and research databases. Experience with technology transfer agreements, clinical trial agreements, cooperative research and development agreements, or related partnerships. Experience supporting NIH, NCI, academic medical centers, or federally funded research programs. Strong communication, organizational, and stakeholder-management skills. Salary $140,000–$150,000 USD
Benefits 100% Medical, Dental & Vision Coverage; PTO and Holidays; 401K match up to 5%; Educational Benefits; Employee Referral Bonus; Flexible Spending Accounts (FSA); Parking Reimbursement; Dependent Care Assistant Program; Transportation Reimbursement A
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Oversee regulatory compliance including IRB submissions, regulatory submissions, audits, and inspections.
Coordinate cross-functional communication among investigators, data managers, regulatory staff, and clinical teams; support governance and decision-making. Requirements Master's degree required; relevant certifications preferred (SOCRA, FAC-P/M, FAC-COR, PMP). Experience with clinical trial management systems and research databases. Experience with technology transfer agreements, clinical trial agreements, cooperative research and development agreements, or related partnerships. Experience supporting NIH, NCI, academic medical centers, or federally funded research programs. Strong communication, organizational, and stakeholder-management skills. Salary $140,000–$150,000 USD
Benefits 100% Medical, Dental & Vision Coverage; PTO and Holidays; 401K match up to 5%; Educational Benefits; Employee Referral Bonus; Flexible Spending Accounts (FSA); Parking Reimbursement; Dependent Care Assistant Program; Transportation Reimbursement A
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Based on: Clinical Program Manager
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