Job Summary:
The Clinical Research Associate I will be responsible for the coordination of clinical research studies within the Department of Orthopedic Surgery. Within this role the scope of duties is but not limited to: 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 and the administration of study questionnaires and assessments. Occasional travel is required. Minimum Qualifications: Bachelor's degree and 2-year's related experience or equivalent combination of education and experience. Preferred Qualifications: Prior experience with clinical research protocols and/or experience with coordinating clinical trials. ACRP and/or SOCRA certification. Work Days: Prior experience with clinical research protocols and/or experience with coordinating clinical trials. ACRP and/or SOCRA certification. Message to Applicants: Salary Range-$60,406-$62,000 RecruitmentOffice: Human Resources...Job Responsibilities: Data Entry: The role involves significant data entry tasks, handling utility outreach, and prioritizing incoming... ...meetings. Candidate Background: The role is open to entry-level candidates with one to three years of work experience and a bachelor...
..., Crossfunctional teams, Vendors and Integration partners. Process knowledge and application understanding of Veeva Align, Veeva CRM, Salesforce is a must with knowledge on Veeva Vault, Network and Nitro considered as added skillsets. Candidate should be proficient...