Study Design Lead – Clinical Research, Central Labs Services

🔥 14 hours ago

🇺🇸 United States – Remote

💵 $70k - $90k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Labcorp

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1969

💼 Consulting

📦 Logistics

🏥 Healthcare

💰 Post-IPO Debt on 2019-06

Consulting • Logistics • Healthcare

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

• Interpret sponsor protocol requirements and translate them into a precise, study-specific database design that drives the creation of the Statement of Work for each CLS project • Apply technical, therapeutic area, client, and CLS process knowledge to deliver complete and accurate database designs • Engage regularly with external clients throughout all phases of study design and development • Partner with internal departments to understand organizational capabilities and evaluate feasibility of client study-design requests • Consult on study-design decisions and collaborate with the Global Study Manager to identify risks and budget implications • Coordinate feasibility assessments, material transfer agreements, supply forecasting, communications, and follow-up actions • Incorporate requirements into the database and global monitoring plan and conduct quality self-review • Document all client study-design requirements and ensure they are addressed • Manage a diverse portfolio of global and local studies with varying complexity

🎯 Requirements

• High School Diploma • 7 or more years of professional experience working in clinical or preclinical research • 1 or more years of experience working directly with clients and stakeholders • Strong scientific acumen with an investigative, analytical mindset • Self-starter with the ability to independently identify and obtain needed information • Familiarity with clinical or preclinical research protocols • Strong planning, organizational, and problem-solving capabilities • Excellent verbal and written communication skills • Proven relationship-building and relationship-management skills • Effective at managing shifting timelines, evolving priorities, and competing demands with clarity and discipline

🏖️ Benefits

• Medical insurance • Dental insurance • Vision insurance • Life insurance • Short-term disability (STD) • Long-term disability (LTD) • 401(k) plan • Paid Time Off (PTO) or Flexible Time Off (FTO) • Tuition Reimbursement • Employee Stock Purchase Plan