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Job type: Permanent

Discipline: VP/Head of Clinical Operations

Location: United States

Clinical Operations Area Director - Permanent - Yukon, OK

Ready to be the heartbeat of clinical operations? Join our client and assist in turning innovative science into life-changing care!

��Ƶ is seeking an Area Director of Clinical Operations to provide strategic leadership and operational oversight across multiple clinical research sites.

Primary Responsibilities:

In this role, you will ensure the successful execution of clinical studies, from start-up through completion, while driving performance, resource optimization, and compliance. This position requires a collaborative leader who can align cross-functional teams, manage risks, and deliver on financial and operational objectives.

Skills & Requirements:

Strong knowledge of regulatory requirements, project management methodologies, and clinical research operations.
Expertise in sponsor engagement, site management, and risk mitigation.
Proven leadership in managing multi-site operations and developing staff.
Exceptional communication, analytical, and problem-solving skills.
Bachelor's degree in a relevant field required; advanced degree preferred.
Experience in clinical research, including supervisory or management roles.
Willingness to travel as needed, including air travel.

The Clinical Operations Area Director's responsibilities will be:

Lead project management for assigned studies, ensuring timelines, milestones, and deliverables are met.
Coordinate cross-functional activities, including site operations, recruitment, regulatory, quality, and sponsor-CRO interactions.
Monitor study performance, proactively addressing barriers to enrollment, timelines, and revenue.
Oversee operational planning for high-priority and multi-site studies, allocating resources effectively.
Drive accountability for area performance, ensuring enrollment milestones and revenue targets are achieved.
Evaluate site and study performance using KPIs and dashboards, identifying trends and opportunities for improvement.
Partner with site leadership to develop corrective action plans for underperforming studies.
Ensure sites have adequate staffing, training, equipment, and resources to execute studies successfully.
Provide oversight of study execution, including visit completion, data entry, and query resolution.
Identify and mitigate operational risks, ensuring quality and compliance standards are upheld.
Report regularly to executive leadership on area performance, risks, and growth opportunities.
Promote a culture of collaboration, accountability, and continuous improvement.

If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

��Ƶ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ��Ƶ is acting as an Employment Agency in relation to this vacancy.

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