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.
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