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About the role

Overview: In this Clinical Lead role you drive the clinical delivery of studies within a global project team, ensuring regulatory compliance, recruitment targets, and high-quality results. You partner with Project Leaders and clinical teams to meet contractual and SOP-based requirements, shaping risk management and stakeholder communications. You influence clinical delivery strategy and, where needed, mentor peers to sustain project success. This is an opportunity to lead cross-functional delivery in a fast-paced, impact-driven environment.
Responsibilities: Ensure clinical delivery in compliance with ICH-GCP, protocol, contracts, SOPs, and project plans Meet recruitment targets and implement effective recruitment strategies Contribute to and manage project risk mitigation throughout the lifecycle Oversee clinical quality delivery and monitor compliance with quality standards Manage project finances related to clinical delivery (including EAC) and identify out-of-scope opportunities Identify and manage clinical stakeholder landscape; maintain effective communication with internal and external stakeholders Collaborate with clinical teams to achieve milestones and report to stakeholders as required Lead resourcing and talent planning for the clinical team; deliver high-quality operational plans and trainings Conduct regular team meetings and provide performance feedback to line managers Contribute to clinical delivery strategy for proposals and participate in bid defense preparations Develop and present Clinical Operation plans in partnership with Business Development and Project Leadership Mentor and coach new peers; work on large, global trials with other Clinical Leads Attend site visits as applicable to support project delivery
Key requirements: Bachelor's Degree in health care or other scientific discipline 5 years of clinical research/monitoring experience or equivalent Basic knowledge of project management practices and terminology Knowledge of GCP/ICH regulatory requirements and broad protocol knowledge Understanding of clinical research industry and regulatory environments Understanding of project finances Experience with clinical trial conduct and applicable regulatory requirements Strong written and verbal communication in English Problem solving, organizational, prioritization, and attention to detail abilities Leadership, mentoring, and training capabilities Proficiency with Microsoft Office (Word, Excel, PowerPoint) Ability to collaborate across geographies and influence without authority IQVIA Core Competencies: Client Focus, Collaboration, Communication, Innovation, Ownership Communication Problem solving Organization Microsoft Word Microsoft Excel Microsoft PowerPoint

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JOB OVERVIEW

Experience level

Manager

Location

Durham, NC

Occupation

Clinical Research Coordinators

Industry

Research and Development in the Physical, Engineering, and Life Sciences

Posted

today

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