Senior Manager, Clinical Operations Site Management – CNS

🔥 18 hours ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

🏥 Clinical Operations

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Provide therapeutic and operational expertise throughout the program/project delivery lifecycle • Ensure that projects within the Franchise are properly resourced • Responsible for collaborating with Therapeutic team to provide effective delivery strategies and solutions for Franchise projects and programs • Act as main contact person for the Project management Franchise Lead • Present at Proposal Defense/client meetings as needed to support new or ongoing business • Ensure LCRAs are trained to support the clinical scope of work (which includes SOP review, QI/CAPA understanding, Clinical Monitoring Plan) • Coordinate and collaborate, with Worldwide Global Quality Assurance, to provide training opportunities identified in CAPA information • Coordinate efforts between the Project Management, Site Management, and Study Start Up • Establishing regular communication to include quality metric (SVR compliance, SDV metrics, on site metric discussion, etc.) and overall "health" of the projects (data query status, managing to the SOW, resource status) • Conduct appraisal performance review for direct reports

🎯 Requirements

• 4-year college curriculum with a major concentration in biological, physical, health, pharmacy or other related science • 8 years clinical research experience as a clinical research associate OR Equivalent education/training and 10 years clinical research experience as a clinical research associate • At least 2 years of management experience • Experience with CNS trials is required for this role

🏖️ Benefits

• We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity • Health insurance • Professional development opportunities