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Clinical Project Manager / Senior Clinical Project Manager
Precision For MedicineClinical Project Manager managing global oncology clinical trials for Precision for Medicine. Ensuring project delivery and client relationship management in a CRO setting.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive experience in clinical project management within a CRO, with a strong understanding of GCP/ICH guidelines and the clinical development process. Proven ability to lead international trials, manage cross-functional teams, and effectively communicate with clients and stakeholders.
Highest-signal resume keywords
Clinical Project ManagementOncology Study ManagementGCP/ICH Guidelines KnowledgeClient Liaison and Presentation SkillsCTMS and EDC Software Proficiency
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Project ManagementClinical OperationsMedical MonitoringData ManagementBiostatisticsProtocol PreparationBudget ManagementPerformance Metrics IdentificationClinical Trial ExecutionStudy Documentation Review
Soft Skills
Interpersonal SkillsOrganizational SkillsCustomer ServiceEffective CommunicationRelationship Building
Tools & Technologies
MS OfficeMS ProjectPowerPointCTMSETMFEDCIXRS
Industry Keywords
Clinical Research OrganisationCRO IndustryClinical Development PlanOncologyClinical Trial Activities
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Independently lead clinical projects in accordance with the study budget and scope of work. You will use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and financial objectives. You may be called upon to run international trials as well.
- Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations
- Liaise with Project Team and senior management of both Precision and sponsors, including C level
- Handle and lead all aspects of a clinical research trial or trials
- Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
- Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.
- Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials
- Prepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets
Requirements
What you’ll need- Degree or similar related life science qualification, or equivalent combination of education and experience.
- Previous experience in a full service/global Project Management role working in the CRO industry is essential.
- Extensive experience working within Clinical Operations position within a CRO, and at least 4 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation.
- Experience managing studies within Oncology
- Working understanding of GCP/ICH guidelines and the clinical development process
- Ability to drive and availability for domestic and international travel including overnight stays
- Be able to communicate effectively in the English language both written and spoken
- Strong presentation skills
- Proven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)
- Proven ability to develop positive working relationships with individual and teams internally and externally
- Demonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan
Benefits
Comp & perks- Remote work options
- Supportive and collaborative environment