Study Design Lead – Clinical Research, Central Labs Services

Source API remote eligibility restrictions: United StatesFull-TimeLead

Salary70,000 - 90,000 USD per year

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Job Details

High School Diploma
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
Bachelor’s degree in a life science (Preferred)

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.
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.
Ensure that all customer requirements with relation to study design are documented and acted upon.
Manage a portfolio of global and local studies with varying complexities.

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