Clinical Research Associate - Clinical Trials Office (Temporary Full Time, 40, Day)

RESPONSIBILITIES I. JOB SUMMARY/RESPONSIBILITIES: Conducts clinical research studies under the immediate direction of assigned Principal Investigator. Assists researchers, clinical and administrative personnel in performing a variety of duties on a research project. II. TYPICAL PHYSICAL DEMANDS: Essential: standing, sitting, walking, seeing, hearing, speaking static gripping of an object for prolonged periods, frequent gripping of an object. Frequent: lifting and carrying usual weight of 2 pounds up to 10 pounds, repetitive arm/hand motions. Occasional: walking on uneven ground, finger dexterity, reaching above, at and below shoulder level. Operates computer, printer, copier, telephone, calculator, facsimile. III. TYPICAL WORKING CONDITIONS: Not substantially subjected to adverse environmental conditions. Must be flexible to accommodate the nature of research (early morning sample collection/preparation). May need to work some nights and weekends. IV. MINIMUM QUALIFICATIONS: A. EDUCATION/CERTIFICATION AND LICENSURE: Bachelor's degree in science or related field. Current certification in BLS/HCP. B. EXPERIENCE: Minimum two (2) years experience working in a research setting. Experience to demonstrate knowledge of research regulatory processes (human subject protection, biological safety, conflict of interest, research misconduct), guidelines, rules and regulations and policies and procedures. Advanced skills in the use of relational databases (e.g., Access,) Excel, Microsoft Office Suite, Adobe. Equal Opportunity Employer/Disability/Vet