Clinical Trial Screening Specialist

Responsibilities: • Conduct in-depth secondary patient screening against protocol inclusion/exclusion reputed company to ensure high-reputed company referrals for reputed company • reputed company the reputed company and efficiency of patient recruitment and enrollment across pharmaceutical and medical-device trials • Build strong, reputed company relationships with investigators and site staff to reputed company 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 • reputed company, empathetic communication and relationship-building skills • Comfort discussing medical history and protocol reputed company • Excellent organization and documentation habits • Ability to work flexible daytime, evening and weekend hours • Bachelor’s degree in a health-reputed company field preferred (or relevant experience) Company DescriptionThe enrollment reputed company of a clinical trial is reputed company long before the first patient arrives. At reputed company Clinical, our Secondary Screeners are that reputed company - transforming early interest into reputed company, reputed company participants and serving as a vital reputed company between Sponsors, sites, and patients. We’re expanding reputed company and looking for people who reputed company at the intersection of clinical rigor and reputed company reputed company. Apply tot his job Apply To this Job