Study Design Lead

This is a fully remote position, open to applicants in Poland.

📋 Description

• Interpret and transform sponsor protocol requirements into databases tailored for protocols to create Statements of Work for Central Lab Services projects.

• Deliver detailed database designs leveraging technical expertise, therapeutic-area knowledge, client specifications, and company processes.

• Maintain regular communication with external clients.

• Collaborate with internal departments to evaluate feasibility and fulfill client requirements regarding study design.

• Provide counsel on study design options and work alongside the Global Study Manager to pinpoint risks and budget considerations.

• Oversee internal study-design processes and communication, which includes feasibility requests, material transfer agreements, and supply forecasting.

• Incorporate follow-up activities into databases and global monitoring strategies.

• Record and respond to customer study-design specifications.

• Conduct quality self-assessments.

• Engage in functional meetings and ensure processes are current.

• Adhere to the Central Lab Global Project Management strategy.

• Manage a portfolio of both global and local studies with varying levels of complexity.

• Promote continuous improvement, quality, and overall productivity.

⛳️ Requirements

• Bachelor’s degree in a life science field.

• A minimum of 6 years of experience in the clinical research sector or within a laboratory setting.

• A Master's degree in a life science is preferred.

• At least 6 years of experience in Central Lab Project Management is preferred.

• Experience in direct interaction with internal or external clients.

• Strong skills in relationship building and management.

• Familiarity with clinical or preclinical research protocols.

• Excellent planning, organizational, and problem-solving abilities.

• Outstanding verbal and written communication skills.

• Proficient in using computer applications, including Windows, Excel, and Word.

• Knowledge and experience in study design techniques related to the creation and maintenance of protocol-specific databases and Statements of Work.

• Capable of managing dynamic timelines, competing priorities, and various study complexities.

🏝️ Benefits

• Commitment to Equal Opportunity Employer principles.

• Consideration for qualified candidates without regard to protected characteristics.

• Disability accommodations for online job searching and applications.

• Access to an accessibility site or Labcorp Accessibility support.

• Opportunities for global career advancement.

• Ability to engage in meaningful work that has a significant impact on people's health.