FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.

Clinical Project Manager
Everest Clinical Research. Manage projects across clinical operations, data management, statistics, medical writing, clinical trial technologies, data monitoring and adjudication committees, and regulatory submissions .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive experience in managing clinical trials across all phases, with a strong understanding of ICH guidelines and regulatory requirements. Proficient in project management, budget estimation, and cross-functional coordination, while effectively communicating with stakeholders and sponsors.
Highest-signal resume keywords
Clinical Trial ManagementProject ManagementRegulatory ComplianceBudget EstimationFluency in Mandarin Chinese
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 ResearchData ManagementStatisticsMedical WritingProject PlanningRisk MitigationChange Order ManagementOncology ExperienceClinical Trial MonitoringCross-Functional Coordination
Soft Skills
Interpersonal CommunicationNegotiation SkillsProblem-SolvingConflict ResolutionLeadership Abilities
Tools & Technologies
Project Management ToolsCommunication PlansTracking SheetsSOPsInformation Repositories
Industry Keywords
ICH GuidelinesFDA RegulationsHealth Canada RegulationsEMA RegulationsClinical OperationsBiotechnologyPharmaceuticalsContract Research OrganizationData Monitoring CommitteesAdjudication Committees
About the role
Key responsibilities & impact- Manage projects across clinical operations, data management, statistics, medical writing, clinical trial technologies, data monitoring and adjudication committees, and regulatory submissions
- Mobilize project teams and track milestones, deliverables, resources, timelines, and overall project success
- Develop project budgets and maintain cross-functional project work plans
- Prepare and facilitate internal and external project kick-off meetings
- Implement project management tools, communication plans, risk mitigation strategies, and tracking sheets
- Lead project management for assigned Phase I to IV clinical trials in accordance with ICH, FDA, Health Canada, EMA, and other applicable requirements
- Schedule and conduct project meetings, communicate assignments and priorities, and track deliverables and training
- Serve as primary point of contact for clinical trial Sponsors
- Coordinate activities across functional teams, Sponsors, and third-party vendors
- Manage project planning, implementation, conduct, reporting, timelines, budgets, and quality
- Track project tasks, hours, budgets, financial status, expenses, out-of-scope work, and Change Orders
- Prepare project status and progress reports and alert management to major risks
- Review client portfolio performance and develop continuous improvement plans
- Generate sales leads and identify opportunities for additional Everest services
- Facilitate problem solving and conflict resolution
- Support Project Management training materials, SOPs, technology enablement, templates, work instructions, and information repositories
- Coordinate RFI and RFP responses, cost estimates, proposals, bid defense materials, Service Work Orders, Change Orders, and project-specific contracts
Requirements
What you’ll need- Bachelor of Science or Master of Science in life sciences or health related field
- Minimum of 8 years of clinical research experience within a pharmaceutical, biotechnology, or contract research organization setting
- Fluency in Mandarin Chinese is required
- Oncology experience is preferred
- Experience as a clinical trial monitor; initiating, monitoring, and closing out clinical trials is desirable for Clinical Operations support tasks
- Demonstrated understanding of cross-functional processes including clinical operations, statistics, data management, subject randomization and drug supply management, data monitoring and adjudication committees, regulatory affairs, and medical writing
- Knowledge and understanding of ICH guidelines, FDA, Health Canada, and EMA regulations
- Ability to define scopes and estimate budgets and plan and manage projects, including resource requirements and utilization, hours spent versus budgets, key deliverables, and timelines
- Demonstrated leadership abilities, including setting goals for others and driving to achieve them in accordance with allocated resources, timelines, and budgets
- Excellent interpersonal, oral, and written communication skills
- Demonstrated strong negotiation and presentation skills
- Strong ability in problem-solving, including conflict resolution
Benefits
Comp & perks- Medical, dental, and vision coverage
- Life & AD&D insurance
- Short- and long-term disability
- Tuition reimbursement
- Fitness reimbursement
- Employee assistance program (EAP)
- Pension plan
- Generous paid time off and sick leave
- Opportunity to earn a performance based bonus
- Remote work from a home-based office anywhere in Canada in accordance with the Work from Home policy