Project Manager
CenExel
full-time
Posted on:
Location Type: Remote
Location: United States
Visit company websiteExplore more
Tech Stack
About the role
- Oversees the planning, execution, and close-out of clinical research studies for single and multi-site studies
- Ensures operational excellence, regulatory compliance, and timely delivery of study milestones
- Leads cross-functional teams through all phases of clinical trial execution
- Develops and manages project timelines and deliverables
- Monitors progress against milestones and proactively addresses risks or delays
- Tracks enrollment metrics, protocol deviations, and site performance
- Optimizes resource allocation and capacity planning
- Coordinates with sponsors, CROs, and internal teams to ensure alignment
- Maintains Trial Master Files (TMF)
- Supports audit readiness and CAPA implementation
Requirements
- Bachelor’s degree in life sciences or related field
- 4+ years of clinical research experience (Project Management experience preferred)
- ACRP certification a plus
- Strong knowledge of FDA regulations and ICH GCP
- Proficiency in SharePoint, Excel, and project management tools
- Experience with multi-site trials and sponsor/CRO collaboration, preferred
- Familiarity with MedDRA coding and pharmacovigilance workflows
Benefits
- Health Insurance
- Dental
- Vision
- LTD
- STD
- Life Ins
- 401k
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical researchproject managementresource allocationcapacity planningenrollment metrics trackingprotocol deviations monitoringsite performance trackingMedDRA codingpharmacovigilance workflowsregulatory compliance
Soft Skills
leadershipcross-functional team collaborationrisk managementcommunicationorganizational skillsproblem-solvingtimely deliveryaudit readinessproactive addressing of delaysalignment coordination
Certifications
Bachelor’s degree in life sciencesACRP certification