Clinical Trial Manager

🕒 April 16

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 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 leadership and direction to clinical site management team members from study start through to closure • Serve as Site Management primary point of contact and representative for clinical monitoring and site activities within the project, including, but not limited to: 1. Primary Sponsor contact 2. Investigator and Bid Defense Meetings 3. Internal and External study team calls 4. Project-specific Audits / Inspections • Manage monitoring deliverables to achieve study budget and identify Out of Scope Activities • Oversee compliance to the Clinical Monitoring Plan, including site visits, outstanding trip reports and visit follow up letters

🎯 Requirements

• Four-year college curriculum or equivalent with a major concentration in biological, physical or health studies and a minimum experience of 3 years as a Senior Clinical Research Associate (or equivalent) • Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree preferred) and a minimum experience of 5 years as a Senior Clinical Research Associate • Minimum 6-month experience functioning as CTM/LCRA (or equivalent); supporting main CTM and coordinating clinical operations activities • Willingness to travel • Excellent interpersonal, oral, and written communication skills in English and in local language • Ability to lead and motivate a team remotely • Demonstrate initiative and problem-solving skills by offering solutions when obstacles are identified • Strong customer focus, ability to interact professionally within a sponsor contact • Proficiency in Microsoft Office, CTMS, and EDC Systems

🏖️ Benefits

• Health insurance • retirement plans • paid time off • flexible work arrangements • professional development