Study Design Lead

🔥 2 hours ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

🎨 Product Designer (UI/UX)

🇬🇧 UK Skilled Worker Visa Sponsor

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Logo of Labcorp

Labcorp

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

• Accurately interpret and translate sponsor protocol requirements into the protocol specific database to generate a Statement of Work for the CLS project. • Leverage technical, therapeutic area, client, and company specific process knowledge to provide a comprehensive and complete database design. • Interact with external clients regularly through all duties and responsibilities. • Liaise with internal departments to understand full company capabilities and assess feasibility of requests to meet client needs related to study design. • Act as a consultant to advise on study design choices and work with the Global Study Manager (GSM) to highlight risks and budget impacts associated with study design. • Expand consultancy capability at study program levels. • Display strong interpersonal and communication skills that will build strong internal and external relationships to ensure high quality study design. • Coordinate internal processes and communications related to study design (including but not limited to internal feasibility requests, material transfer agreements and supply forecasting) and ensure the eventual follow up is integrated into the database and global monitoring plan. • Perform quality self-review. • Ensure that all customer requirements with relation to study design are documented and acted upon. • Act efficiently in an environment with dynamic timelines and priorities. • Display appropriate self-organization and ability to manage conflicting priorities. • Participate in functional meetings (e.g. Continuous Learning Forums (CLFs)) and provide input, keeping processes up to date. • Comply with our internal Central Lab Global Project Management strategy. • Manage a portfolio of global and local studies with varying complexities. • Support a culture of continuous improvement, quality, and productivity.

🎯 Requirements

• Bachelor’s degree in a life science • 6 or more years of experience working in the clinical research industry or within a lab environment • Experience working directly with internal or external customers • Strong relationship building and management skills • Familiarity with clinical or preclinical research protocols • Strong planning, organizational, and problem-solving skills • Excellent verbal and written communication skills • Excellent skills using computer applications (e.g. Windows, Excel, Word).

🏖️ Benefits

• Inclusion and belonging in the workforce • Equal Opportunity Employer.

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