Labcorp is seeking a Study Design Lead to accurately interpret and translate sponsor protocol requirements into the protocol specific database, working directly with the client, to support global clinical trials testing.
Requirements
- Strong planning, organizational, and problem solving skills
- Excellent verbal and written communication skills required
- Six (6) years of previous experience in Central Lab Project Management or other equivalent industry experience
- Bachelor’s degree in a life science is strongly preferred
- Ability to work in an environment with dynamic timelines and priorities
- Ability to display appropriate self-organization and ability to manage conflicting priorities
Responsibilities
- Leverage technical, therapeutic area, client, and company specific process knowledge to provide a comprehensive and complete database design
- Act as a consultant to the client to advise on study design choices and works with the Global Study Manager (GSM) to highlight risks and budget impacts associated with 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
- Manage a portfolio of global and local studies with varying complexity
- Support a culture of continuous improvement, quality, and productivity
- 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
Other
- Bachelor’s degree in a life science is strongly preferred
- Six (6) years of previous experience in Central Lab Project Management or other equivalent industry experience
- Excellent verbal and written communication skills required
- Ability to work in an environment with dynamic timelines and priorities
- Travel requirements not specified
