Job Description
Job Description
Responsibilities:
*Conduct in-depth secondary patient screening against protocol inclusion/exclusion criteria to ensure high-quality referrals
*Elevate the quality and efficiency of recruitment across pharmaceutical and medical-device trials
*Build strong, professional relationships with investigators and site staff to keep trials “top of mind”
Qualifications:
*1–3+ years in clinical research, patient recruitment, or healthcare
Experience reviewing medical records and/or performing pre-screening
*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.
Company Description
The 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.\n\nWe’re expanding our team and looking for people who thrive at the intersection of clinical rigor and human connection.