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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in trial management, including site feasibility, recruitment strategy, and compliance with ICH-GCP standards. Proficient in managing complex Early Phase trials and maintaining strong communication with stakeholders and site staff.
Highest-signal resume keywords
Trial ManagementICH-GCP KnowledgeHemOnc ExperienceBudget ManagementSite Recruitment Strategy
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Trial ManagementSite FeasibilityBudget ForecastingData Quality ManagementCAPA ImplementationInformed Consent PreparationVendor ManagementDatabase LockingRisk ManagementStudy Documentation
Soft Skills
Communication SkillsTeam CollaborationProblem SolvingStakeholder EngagementTraining Facilitation
Tools & Technologies
CTMSETMFTrial Management SystemsLocal Study Supplies ManagementMonitoring Training Tools
Industry Keywords
Clinical TrialsHealth SciencesRegulatory ComplianceAdverse Event ReportingInspection Readiness
About the role
Key responsibilities & impact- Serve as the primary point of communication for assigned trial sites and facilitate internal client teaming to drive issue resolution
- Maintain relationships with critical site stakeholders and provide a voice for sites to client teams
- Contribute to site feasibility, site qualification visits, follow-up, and final site selection
- Coordinate local team activities, recruitment planning, contingency and risk management, budget forecasting, and study-level documentation
- Engage investigators and site staff throughout the trial and communicate status information and issues to stakeholders
- Maintain and update trial management systems and analyze trial progress
- Initiate corrective and preventive actions when trials deviate from plans
- Contribute to site-level recruitment strategy and contingency planning
- Manage country-level vendors, invoices, local study supplies, and vendor selection requests
- Conduct local trial team meetings and facilitate monitoring training
- Prepare and manage country- and site-specific informed consent forms
- Ensure adverse events, serious adverse events, and product quality complaints are reported within required timelines
- Maintain inspection readiness, essential documents, CTMS and eTMF/IF data, and archive records
- Ensure site data quality and timely query resolution
- Support CAPA implementation for audits, inspections, and quality visits
- Ensure accurate finance reporting and proactive country/local budget management
- Organize IEC/HA approvals with the local Start Up team
- Provide systems/process training and contribute to process initiatives
- Complete timely and accurate time reporting
- Manage complex Early Phase trials with internal matrix clinical teams and sites
Requirements
What you’ll need- BA/BS degree
- Degree in a health or science related field
- 3 - 5+ years of trial end to end management experience
- Start-up & Database Locks/Cleaning experience preferred
- HemOnc experience required
- Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures
- Strong IT skills in appropriate software and company systems
- Proficient in speaking and writing the country language and English
- Good written and oral communication skills as appropriate
- Legally authorized to work in the United States
- Must not require, now or in the future, sponsorship for employment visa status
Benefits
Comp & perks- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
