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.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive experience in clinical research management, ensuring compliance with ICH/GCP and local regulations while effectively leading study teams and managing project deliverables. Proficient in strategic planning, risk management, and fostering relationships with stakeholders to drive successful clinical trial outcomes.
Highest-signal resume keywords
Clinical Research ManagementICH GCP ComplianceProject ManagementTeam LeadershipRisk Management
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 PlanningClinical Trials MonitoringClinical Trials OperationsRegulatory ComplianceQuality ManagementMetrics AnalysisResource AllocationProtocol DevelopmentBudget ManagementTraining and Development
Soft Skills
Strong Organizational SkillsStrategic ThinkingSkilled NegotiationConflict ResolutionEffective Communication
Tools & Technologies
CTMSETMF
Industry Keywords
Clinical ResearchAdverse Event ReportingFeasibility StudiesSite ManagementOutsourcing Vendors
About the role
Key responsibilities & impact- Serve as the main point of contact for assigned protocols and link Country Operations with the clinical trial team
- Plan, drive, and track study deliverables, timelines, and results from feasibility and site selection through recruitment, execution, and closeout
- Ensure assigned protocols comply with ICH/GCP, country regulations, company policies, quality standards, and adverse event reporting requirements
- Review Monitoring Visit Reports and escalate performance issues and training needs
- Perform Quality Control visits as required
- Lead local study teams, train local roles, support CRAs as protocol expert, and coordinate country activities
- Create and execute local risk management plans
- Ensure compliance with CTMS, eTMF, and other key systems
- Escalate challenges and issues to appropriate clinical research and quality leadership
- Collaborate with outsourcing vendors, investigators, and external partners
- Serve as country point of contact for programmatically outsourced trials
- Support local business needs, including signing contracts and managing budgets when delegated
- Collaborate with headquarters, Pharmacovigilance, Regulatory, and Global Medical Affairs functions
- Build business relationships with investigators and represent the company in a customer-facing role
- Share protocol-specific information and best practices across countries and clusters
- Manage end-to-end performance and project management for assigned clinical research protocols
Requirements
What you’ll need- 5+ years of experience in clinical research
- Bachelor’s degree in science or comparable qualification
- Knowledge in project management and site management
- Strong organizational skills
- Ability to make independent decisions and oversee clinical research activities according to global policies
- Strong understanding of the local regulatory environment
- Strong scientific and clinical research knowledge
- Understanding of clinical trial planning, management, and metrics
- Ability to manage multiple deliverables and protocols simultaneously
- Effective written and spoken English and local language proficiency
- Ability to manage resource allocation, processes, productivity, quality, and project delivery
- Strategic thinking
- Strong leadership skills
- Ability to identify problems, conflicts, and opportunities and prepare mitigation plans
- Skilled negotiation and conflict resolution
- Educational, diplomatic, and empathic skills for maintaining professional relationships
- Knowledge of Clinical Quality Management, Clinical Trial Planning, Clinical Trials Monitoring, Clinical Trials Operations, ICH GCP Guidelines, Regulatory Compliance, Risk Management, Strategic Planning, Team Leadership, and Training and Development
- No visa sponsorship available
- Valid driving license is not required
Benefits
Comp & perks- Annual bonus eligibility
- Long-term incentive eligibility, if applicable
- Medical, dental, and vision healthcare
- Other insurance benefits for employee and family
- Retirement benefits, including 401(k)
- Paid holidays
- Vacation days
- Compassionate and sick days
- Remote work arrangement
- 25% travel requirement
- No relocation required
