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...please wear it as often as possible. Dress for success. "Look good, feel good, train good." Training Protocol: Follow the... ...studio that provides clients with a winning edge in their respective sports or individual goals. Each client is taken through a...
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...Description Eurofins Biopharmaceutical is looking for an Associate Scientist to support Data Review of our Biochemistry team. The Associate Scientist position is considered an entry-level opportunity that will allow for hands on development and growth in day-...
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