Job Summary:

Coordination of ALS 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 ALS 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.

Minimum Qualifications:

Bachelor's degree and two years of related experience or equivalent combination of education and experience. Working knowledge of medical terminology, basic computer skills and excellent written/oral communication and organizational skills

Preferred Qualifications:

Prior experience with clinical research protocols and/or experience with
coordinating ALS clinical trials. ACRP and/or SOCRA certification.

Work Days:

Mon- Fri 8-4:30 with occasional after hours

Message to Applicants:

Recruitment Office: Human Resources