Clinical Project Manager – Early Clinical Development

🔥 7 hours ago

🌪️ Kansas, Kentucky, +8 more states – Remote

🌪️ Kansas – Remote 🐎 Kentucky – Remote ⚜️ Louisiana – Remote 🏖️ New Jersey – Remote 🗽 New York – Remote 🏈 Ohio – Remote 🚗 Michigan – Remote 🏰 Missouri – Remote 🔔 Pennsylvania – Remote ⚔️ Virginia – Remote

💵 $93.1k - $232.8k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🏥 Clinical Operations

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Plan, implement, and execute contracted clinical trial activities • Manage full-scope regional and global projects and lead project teams • Build and maintain positive client relationships • Negotiate with clients while maintaining IQVIA Biotech operational processes and project scope • Review study trends and proactively respond to clients and team members • Develop early warning systems for project obstacles and create solutions • Identify, define, and document training requirements in LMS systems and ensure compliance • Manage change across assigned projects • Ensure projects follow SOPs, working practices, contracts, and timelines • Identify processes requiring updates and communicate them to management • Maintain client relationships, current project reporting, and executive management awareness • Develop, document, and update internal processes, SOPs, working practices, and quality assurance forms • Provide project support to managers and oversee delegated support staff activities • Assist with capability and proposal defense presentations • Support Contracts and Proposals with final contract execution and CIS documentation • Participate in performance appraisals by providing feedback on team members • Maintain knowledge of FDA regulations, GCP, and ICH Guidelines for clinical research • Provide backup project management coverage during absences

🎯 Requirements

• Nursing or University degree (US Bachelor Level or equivalent) in a health-related field with a minimum of three (3) years direct clinical trial experience in a CRO or research-related organization with at least one (1) year management experience OR equivalent level of education and experience • Previous experience in managing people within a scientific/clinical environment is preferred • Clinical Monitoring or Data Management experience required • Excellent and demonstrated verbal and written communication and presentation skills • Ability to work independently, prioritize and work within a matrix team environment • Working knowledge of Word, Excel, and PowerPoint required • Prior experience in electronic data capture preferred • Experience in contract/timeline management preferred • Ability to travel domestically or internationally as required • Knowledge of clinical research processes from Phase I through regulatory submission • Working knowledge of current ICH GCP guidelines • Must be able to secure a credit card cosigned by IQVIA Biotech • Must maintain current currency documentation for IQVIA Biotech SOPs, CAPA completion, and timesheet maintenance

🏖️ Benefits

• Potential incentive plans, bonuses, and/or other forms of compensation • Health and welfare benefits • Home-based work arrangement • Up to 20% travel, including international travel

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