Project Manager, Internal Medicine

🔥 14 hours ago

🌐 United States, Canada – Remote

🇺🇸 United States – Remote 🇨🇦 Canada – Remote

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $112k - $222k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

👷‍♀️ Project Manager

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

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

• Manage one or more allocated Phase I through IV clinical trials with local, regional, or global scope • Coordinate and manage clinical trials from start-up through closeout • Direct the technical, financial, and operational aspects of projects • Identify and evaluate project requirements, interpret complex data, and develop contingency plans and rescue strategies • Ensure project deliverables meet customer time, quality, cost, and contract expectations • Lead core project team members and facilitate leadership of extended or complete project teams • Lead internal and external cross-unit coordination, including subcontractors • Define and manage project resource needs with functional heads and establish contingency plans • Design, implement, track, and revise project plans • Promote effective teamwork and resolve conflicts • Ensure appropriate communication with Project Management leadership

🎯 Requirements

• University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution, or equivalent combination of education and experience • Minimum of five (5) years of clinical pharmaceutical industry experience, including clinical project management tasks • Alternatively, more than five (5) years of supervisory experience in a health care setting and four (4) years of clinical research experience in the pharmaceutical or CRO industries, or proven relevant clinical development experience and skills • Experience managing projects in a multi-office environment • Ability to handle multiple competing priorities and utilize resources effectively • Ability to inspire teamwork and motivate staff within a matrix system • Ability to lead by example and encourage team members to seek solutions • Excellent communication, planning, and organizational skills • Self-motivated with excellent problem-solving skills • Thorough knowledge of project management processes • Thorough knowledge of ICH Guidelines and GCP, including international regulatory requirements • Available for domestic and international travel, including overnight stays • Valid current passport required • Ability to drive and have a valid driver’s license • Fluent in local office language and English, written and verbal • Broad knowledge of drug development processes and client needs

🏖️ Benefits

• Competitive benefits package depending on location • Inclusive and equitable workplace • Transparent compensation and pay equity