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Senior Clinical Project Manager
ClinChoiceSenior Clinical Project Manager overseeing execution of complex clinical trials for a global CRO. Leading cross-functional teams to ensure project delivery and compliance with regulatory requirements.
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
clinical trial managementstudy data documentationbudget managementproject coordinationregulatory complianceGCP guidelinesICH guidelinescomplex study managementscientific knowledgedata management
Soft Skills
leadershipcommunicationinterpersonal skillsorganizational skillsteam managementproblem-solvingtime managementadaptabilitycollaborationperformance monitoring
Tools & Technologies
Microsoft OfficeWordExcelOutlook
Industry Keywords
CRO environmentclinical operationscontractual commitmentsscientific aspectsregulatory requirementsclinical projectsmedical disciplinesparamedical disciplinesNursing degreegeneral medicine studies
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- lead cross-functional teams and oversee the execution of complex clinical trials
- ensure successful delivery in accordance with contractual commitments, SOPs, ICH-GCP guidelines, and applicable regulatory requirements
- manage and coordinate assigned clinical projects
- manage all project-specific services required by the Sponsor
- interact with Sponsor and Investigators and properly coordinate project team members
- keep abreast of all scientific, regulatory, and operational aspects relevant to clinical projects
- collect and manage study data documentation
- assure proper timelines of assigned projects
- manage the budget for the project
- monitor workload and performance of project team
Requirements
What you’ll need- 8+ years of clinical trial management experience
- prior experience within a CRO environment
- experience managing complex studies and/or general medicine studies
- Bachelor's Degree or equivalent in scientific and/or medical or paramedical disciplines; Nursing degree or relevant background preferred
- excellent knowledge of clinical trial operations, GCP/ICH Guidelines and other applicable regulatory requirements
- fluent in English
- proficiency in Microsoft Office (e.g. Word, Excel, Outlook).
Benefits
Comp & perks- health insurance
- strong work-life balance
- professional development