Clinical Operations Area Director

Proclinical; Schweiz; Vor Ort; CAD 185.000 - 257.000; Vollzeit

Zusammenfassung

Proclinical is seeking an Area Director of Clinical Operations to provide strategic leadership and oversee multi-site studies across the assigned region. You will drive timelines, budgets, and quality while partnering with site leadership and sponsor-CRO teams.

Occasional travel will be required to ensure seamless study execution and regulatory compliance. Lead cross-functional coordination, manage risks, and optimize resources to meet enrollment milestones and financial targets.

Qualifikationen

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

Aufgaben

• Lead project management for assigned studies, ensuring timelines, milestones, and deliverables are met.
• Coordinate cross-functional activities across site operations, regulatory, quality, and sponsor-CRO interactions.
• Monitor study performance; proactively address enrollment, timelines, and revenue barriers.
• Oversee operational planning for high-priority, multi-site studies with resource allocation.
• Drive accountability for area performance; achieve enrollment milestones and revenue targets.
• Evaluate site performance using KPIs and dashboards; identify improvement opportunities.
• Partner with site leadership to develop corrective action plans for underperforming studies.
• Ensure sites have staffing, training, equipment, and resources to execute studies.
• Provide oversight of study execution, including visits, data entry, and query resolution.
• Identify and mitigate operational risks; uphold quality and compliance standards.
• Report regularly to executive leadership on area performance, risks, and growth.
• Promote collaboration, accountability, and continuous improvement culture.

Kenntnisse

Regulatory knowledge

Clinical operations

Sponsor engagement

Site management

Leadership multi-site

Communication skills

Problem-solving

Travel readiness

Project management

Ausbildung

Bachelor's degree in a relevant field

Advanced degree preferred

Jobbeschreibung

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!

Proclinical 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.