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...skills to do something more meaningful?We are looking for a Sales Associate to join our team for pre-need sales, as well as at-need cemetery sales. Are you ready for a career that gives you the freedom to openly live out your values, foster your spiritual life, and...
...Area Manager Beaumont Office Schedule: Full-Time / Temp-to-Hire/ MondayFriday, 8:00... ...officials. The Area Manager works closely with legal counsel and clients to achieve... ...other public officials Manage special projects, office operations tasks, and client communications...
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