Clinical Study Coordinator

Duties and Responsibilities

• Day-to-day “hands on” work associated with in-house clinical studies
• Cook up execution of site contracts and site budget preparation
• Process invoices for payment and track project specific budgets and spending
• Cook up coordination and tracking of clinical supplies shipped and used at clinical sites
• Collect and analyze experimental data generated in-house and externally
• Assist with site qualification processes and support monitoring of external clinical sites in accordance with study protocols and applicable regulations and standards (eg. 21 CFR Part 812, GLP, CLSI, ICH)
• Develop study tools and forms (eg. Enrollment logs, Data Record Forms, Case Report Forms etc.)
• Cook up collaboration with sample bank to acquire and dispense clinical specimens for use at external clinical sites
• Maintain study documentation and data history files
• Maintain working knowledge of current protocols and internal SOPs
• Interact with other internal Luminex departments and external service providers, if required (eg. Sequencing facilities, CROs)
• Additional Product Development & Clinical tasks, as need arises
• Other duties as assigned

Education, Experience, and Qualifications

• Bachelor's Degree technical subject plus at least 3 years' work experience. required or
• Bachelor's Degree in chemistry, biology, molecular biology or a related subject, with additional post-graduate diploma or ≥ 1 year work experience preferred but not required; preferred or
• Master's Degree technical subject plus at least 2 years' work experience; preferred
• 1+ Years Previous work experience with clinical trials, analytical or method validation studies preferred. preferred
• Excellent communication, organizational and time management skills
• Proficiency with Microsoft Office software

What we offer

We offer a competitive rewards package focused on your overall well-being. We are proud to offer a comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks. Benefits may vary by role, country, region, union status, and other employment status factors. You may also be eligible to participate in an annual incentive program. An incentive award, if any, depends on various factors, including, individual and organizational performance.

Diasorin is committed to building a workplace where people feel empowered to contribute ideas, take ownership, and grow their careers. We believe diverse perspectives strengthen innovation and help us deliver meaningful impact for patients and customers worldwide.

Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by applicable law.