Clinical Research Associate 2, Sponsor Dedicated

Yesterday

🏄 California – Remote

Although this job is listed in California, this company may be open to hiring remote in other states.

🌪️ Kansas – Remote

Although this job is listed in Kansas, this company may be open to hiring remote in other states.

+1 more states

🏄 California – Remote 🌪️ Kansas – Remote 🌲 North Carolina – Remote

💵 $71.9k - $169.3k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

🦅 H1B Visa Sponsor

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IQVIA

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Healthcare Insurance • Biotechnology • Artificial Intelligence

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.

10,000+ employees

⚕️ Healthcare Insurance

🧬 Biotechnology

🤖 Artificial Intelligence

💰 $1G Post-IPO Debt on 2023-05

📋 Description

• Perform monitoring and site management work to ensure that sites are conducting the study(ies). • Perform site monitoring visits (selection, initiation, monitoring and close-out visits). • Work with sites to adapt, drive and track subject recruitment plan. • Administer protocol and related study training to assigned sites. • Evaluate the quality and integrity of study site practices. • Manage the progress of assigned studies by tracking regulatory submissions and approvals. • Ensure copies/originals site documents are available for filing in the Trial Master File. • Create and maintain appropriate documentation regarding site management. • Collaborate and liaise with study team members for project execution support.

🎯 Requirements

• Bachelor's Degree in scientific discipline or health care preferred. • Equivalent combination of education, training and experience may be accepted in lieu of degree. • Some organizations require completion of CRA training program or prior monitoring experience. • Basic knowledge of clinical research regulatory requirements (i.e., GCP and ICH guidelines). • Good therapeutic and protocol knowledge. • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint. • Written and verbal communication skills including good command of English language. • Organizational and problem-solving skills. • Effective time and financial management skills. • Ability to establish and maintain effective working relationships.

🏖️ Benefits

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