Manager, Clinical Trial Managers – CNS

🕒 5 days ago

🏄 California – Remote

🏄 California – Remote

💵 $112k - $222k / year

⏰ Full Time

🟠 Senior

🔴 Lead

🧪 Clinical Research

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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 and project delivery lifecycle • Ensure that projects within the franchise are properly resourced • Collaborate with the therapeutic team to create effective delivery strategies and solutions for franchise projects and programs • Act as the main contact person for the Project Management Franchise Lead • Present at proposal defense and client meetings as needed to support new or ongoing business • Ensure CRAs are trained on project specifics • Ensure Lead CRAs (LCRAs) are trained to support the clinical scope of work, including standard operating procedure (SOP) review, quality issue (QI)/corrective and preventive action (CAPA) understanding, and the Clinical Monitoring Plan • Coordinate and collaborate with Worldwide Clinical Trials Global Quality Assurance to provide training opportunities identified through CAPA information • Manage the quality of the assigned staff’s clinical work • Coordinate efforts between Project Management, Site Management, and Study Start‑Up • Establish regular communication to include quality metrics (such as site visit report compliance, source data verification metrics, and on‑site metrics) and overall project “health” metrics (such as data query status, adherence to the scope of work, and resource status) • Conduct performance appraisals for direct reports

🎯 Requirements

• Four‑year college curriculum with a major concentration in biological, physical, health, pharmacy, or other related sciences, and eight years of clinical research experience as a clinical research associate, OR Equivalent education and training with ten years of clinical research experience as a clinical research associate • Two or more years of line management experience • Extensive CNS experience required • Experienced in being a direct point-of-contact for Sponsors • Responsibility for metrics and troubleshooting • Extensive budgetary responsibilities required • Travel required • Passport required

🏖️ Benefits

• Competitive benefits package depending on location • Pay equity and transparency