Senior Clinical Project Manager — Remote-Eligible Lead
Voiantclinical
United States
On-site
USD 90,000 - 120,000
Full time
14 days+
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Benefits offered by this job
Comprehensive health, vision, and dental insurance
Generous paid time off and holiday
401(K) with employer matching
Tuition Reimbursement
Internet allowance for remote workers
Community Service Opportunities
Job summary
Voiantclinical is seeking a Senior Clinical Project Manager to provide strategic operational leadership across clinical trials in the United States. The role involves overseeing complex studies, managing staff, developing training programs, and ensuring compliance with regulatory standards. Candidates should have 5-10 years of clinical trial experience, strong project management skills, and a relevant degree. Benefits include comprehensive health insurance, generous PTO, 401(K) matching, and ongoing training opportunities.
Qualifications
Minimum 5–10 years of progressive clinical trial experience within a CRO or pharmaceutical setting.
Minimum 2 years of people management experience.
Demonstrated project management abilities in clinical research.
Strong understanding of regulatory frameworks including ICH GCP.
Responsibilities
Oversees a portfolio of complex clinical studies, ensuring timely and quality delivery.
Develops and executes project plans and supports governance preparation.
Maintains accountability for project health and leads recovery planning.
Manages team performance and development through coaching and feedback.
Standardizes project management processes across service lines.
Skills
Leadership
Project management
Stakeholder management
Communication
Financial acumen
Compliance knowledge
Education
Bachelor’s degree in life sciences, pharmacy, nursing, or related healthcare field
ACRP-PM, PMP, or equivalent certification
Tools
Microsoft Office Suite
CTMS tools
Job description
Voiantclinical is seeking a Senior Clinical Project Manager to provide strategic operational leadership across clinical trials in the United States. The role involves overseeing complex studies, managing staff, developing training programs, and ensuring compliance with regulatory standards. Candidates should have 5-10 years of clinical trial experience, strong project management skills, and a relevant degree. Benefits include comprehensive health insurance, generous PTO, 401(K) matching, and ongoing training opportunities.