Clinical Project Lead, Oncology

IQVIA

Clinical Project Lead overseeing country-level clinical trial operations for a leading clinical research provider. Ensuring high-quality data delivery and compliance with regulatory standards across multiple locations.

Posted 7/30/2026full-timeParsippany • New Jersey, North Carolina, Pennsylvania • 🇺🇸 United StatesSenior💰 $68,400 - $232,800 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial management, ensuring compliance with ICH-GCP and regulatory standards while effectively leading cross-functional teams to achieve recruitment and performance targets.

Highest-signal resume keywords

Clinical Trial ManagementICH-GCP ComplianceStakeholder ManagementCTMS ProficiencyCross-Functional Team Leadership

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Trial ManagementRegulatory RequirementsData DocumentationSite FeasibilityPatient Safety ReportingBudget ManagementFinancial TrackingRecruitment StrategyCorrective And Preventive ActionsStudy Execution

Soft Skills

Excellent CommunicationStakeholder Management

Tools & Technologies

CTMSETMF

Industry Keywords

Clinical ResearchLife SciencesHealthcareRegulatory StandardsSite Activation

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Lead end-to-end country-level trial management, from study start-up through database lock and closeout
Serve as the primary contact for assigned clinical trials within your country
Ensure delivery of high-quality, compliant data and documentation aligned with ICH-GCP, SOPs, and regulatory standards
Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target
Partner with CRA’s, Global Project Leads, and cross-functional teams to ensure successful study execution
Lead site feasibility, selection, and activation processes
Drive investigator engagement and site performance, including recruitment and retention strategies
Monitor study progress through systems and reports; implement corrective and preventive actions (CAPA) when needed
Ensure inspection readiness through complete and accurate trial documentation (CTMS, eTMF)
Oversee patient safety reporting (AEs/SAEs) within required timelines
Manage country-level budgets, forecasting, and financial tracking
Oversee local vendors and site payments, ensuring timely and accurate processing
Coordinate ethics and regulatory submissions/approvals in collaboration with start-up teams
Ensure compliance with local regulations and global standards (ICH-GCP)

Requirements

What you’ll need

Bachelor’s degree in life sciences, healthcare, or related field
Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial processes
Excellent communication and stakeholder management skills
Proficiency in clinical systems (e.g., CTMS, eTMF)
3–5+ years of total trial management experience
Experience managing complex or early-phase trials
Demonstrated ability to lead cross-functional teams and drive performance

Benefits

Comp & perks

Health insurance
401(k) matching
Flexible work arrangements