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Associate Director, Clinical Project Management
CTI Clinical Trial and Consulting Services. Lead management of multiple Phase I-IV clinical research trials across geographic and functional areas .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive experience in managing Phase I-IV clinical trials, ensuring compliance with ICH guidelines and GCP, while effectively leading project teams and overseeing trial operations, budgets, and timelines.
Highest-signal resume keywords
Clinical Trial ManagementICH Guidelines ComplianceGood Clinical Practices (GCP)Project ManagementTherapeutic Area Expertise
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 ResearchProject PlanningBudget ManagementQuality AssuranceResource AssessmentProcess ImprovementData AnalysisContract ManagementMetrics TrackingStaff Training
Soft Skills
LeadershipCommunicationProblem-SolvingMentoringCollaboration
Industry Keywords
Clinical TrialsPhase I-IV TrialsRegulatory GuidelinesClinical Project ManagementTrial Procedures
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Lead management of multiple Phase I-IV clinical research trials across geographic and functional areas
- Plan, implement, facilitate and evaluate assigned clinical trials from planning through analysis and client delivery
- Oversee clinical trial operations, activities, deliverables, timelines, budgets and quality
- Ensure compliance with ICH guidelines, GCP, regulatory guidelines and trial procedures
- Coordinate Clinical Project Managers, Clinical Project Coordinators, functional teams and clients
- Serve as senior interface with CTI executive management and sponsors
- Identify, escalate and resolve trial, staffing and organizational issues
- Prepare and oversee study plans, project timelines, status reports, meeting agendas and minutes
- Assess resource needs and establish project teams
- Track project progress, metrics, budgeted hours and scope against contractual agreements
- Support scope changes, contract amendments, new business proposals, budgeting, presentations and business development
- Train, supervise, guide and mentor CPMs and CPC staff
- Review quality assurance reports and ensure corrective actions
- Lead process improvement initiatives and develop reference and resource materials
- Keep CTI executive management and clients informed of project progress and issues
Requirements
What you’ll need- Bachelor’s degree in an allied health field such as nursing, pharmacy or health science, preferably with clinical trial management experience, or an equivalent combination of education and relevant work experience
- At least 10 years of clinical research experience and/or clinical project management experience
- Clear and thorough understanding of global trial management processes and the operation of all clinical trial functional areas
- Experience managing clinical trials
- Thorough and current understanding of at least one therapeutic area for which CTI is contracted for clinical projects preferred
- Knowledge of ICH guidelines, Good Clinical Practices (GCP), applicable regulatory guidelines and trial procedures
Benefits
Comp & perks- Up to $25K sign-on bonus
- Structured mentoring program
- Leadership development courses
- Ongoing education and training opportunities
- Tuition reimbursement
- Generous health benefits
- Vacation packages
- Hybrid work opportunities
- Paid parental leave
- CTI Cares community and global volunteering opportunities
- Professional growth and career development support