Job Summary:
Coordination of clinical research studies. Performance of regulatory tasks including IRB and sponsor/CRO regulatory correspondence. Communication with IRBs, sponsors, and protocol-related Upstate Departments. Pre-screen, Screen, and enroll research participants in outpatient and inpatient clinical trials. Process and ship lab samples. Schedule and conduct follow up research appointments for clinical trial participants. Data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory. Processing clinical trial billing and payments. Administration of study questionnaires and assessments. Occasional travel. Minimum Qualifications: A bachelors degree and 2 years of related experiance or an equivalent combination of education and experiance. Preferred Qualifications: Prior experience with clinical research protocols and/or experience with coordinating clinical trials. Work Days: Mon - Fri - Daytime hours - occasional weekends/evenings. Message to Applicants: Salary Range-$60,406-$65,000 RecruitmentOffice: Human Resources...comfortable, how comfortable would you be approaching someone and asking them to take a survey? Education: ~ High school or equivalent (Preferred) Experience: Sales: 2 years (Preferred) Customer service: 2 years (Preferred) Work Location: On the road...
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