Clinical Trial Screening Specialist
Responsibilities: • Conduct in-depth secondary patient screening against protocol inclusion/exclusion criteria to ensure high-quality referrals for clinical trials • Elevate the quality and efficiency of patient recruitment and enrollment across pharmaceutical and medical-device trials • Build strong, professional relationships with investigators and site staff to keep trials “top of mind” • Ability to work 20+ hours per week Qualifications: • 3+ years in clinical research (experience as a Clinical Research Coordinator or Clinical Research Associate is a plus) • Experience and confidence working with clinical trial protocols • Clear, empathetic communication and relationship-building skills • Comfort discussing medical history and protocol criteria • Excellent organization and documentation habits • Ability to work flexible daytime, evening and weekend hours • Bachelor’s degree in a health-related field preferred (or relevant experience) Company DescriptionThe enrollment engine of a clinical trial is built long before the first patient arrives. At Link Clinical, our Secondary Screeners are that engine - transforming early interest into qualified, engaged participants and serving as a vital bridge between Sponsors, sites, and patients. We’re expanding our team and looking for people who thrive at the intersection of clinical rigor and human connection. Apply tot his job