Clinical Trials Site Support Associate

Job not on LinkedIn

🔥 1 hour ago

🇺🇸 United States – Remote

💵 $24 - $36 / hour

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Associate

🚫👨‍🎓 No degree required

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Labcorp

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1969

💊 Pharmaceuticals

🧬 Biotechnology

💰 Post-IPO Debt on 2019-06

Healthcare • Pharmaceuticals • Biotechnology

Labcorp is a leading global life sciences company that provides comprehensive clinical laboratory and end-to-end drug development services. The company offers a wide range of diagnostic tests and services for patients, providers, and biopharmaceutical companies. Labcorp specializes in areas such as oncology, women's health, neurology, and genetics, offering both routine and specialized laboratory testing. It supports healthcare systems and organizations with clinical lab testing, health assessments, and employee wellness programs. Labcorp also plays a significant role in the biopharma sector, providing nonclinical research, central laboratory services, and consulting for drug development and commercialization. With their commitment to science and innovation, Labcorp aims to improve health and change lives worldwide.

📋 Description

• Serve as the primary point of accountability for all day-to-day investigator site support activities. • Manage and resolve issues related to incoming study samples for assigned projects, ensuring timely and accurate processing. • Coordinate with Project Managers to ensure the accurate and timely delivery of study supplies to clients. • Collaborate with specimen management teams across all locations to identify, escalate, and resolve issues. • Review, communicate, and distribute abnormal test results in accordance with established protocols and PSW designation. • Partner with cross-functional project teams to troubleshoot and resolve issues related to specimen handling, result reporting, and site compliance. • Engage with appropriate stakeholders to address challenges related to study setup, reporting processes, and regulatory compliance. • Maintain and effectively utilize all tracking systems, tools, and databases required to support operational activities. • Establish, maintain, and ensure the accuracy of study files and documentation in compliance with departmental and regulatory requirements. • Perform all responsibilities in accordance with standard operating procedures (SOPs), policies, and quality standards.

🎯 Requirements

• HS diploma, degree in science related field or experience in specimen management, client services or other related laboratory positions • 2 or more years’ experience of clinical trials in Specimen Management, client services or other laboratory positions • 2 or more years’ experience in customer service experience within a clinical Lab setting • Excellent organizational and communication skills • Proficient in MS Office applications

🏖️ Benefits

• Medical • Dental • Vision • Life • STD/LTD • 401(k) • Paid Time Off (PTO) or Flexible Time Off (FTO) • Tuition Reimbursement • Employee Stock Purchase Plan