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

Responsibilities

Review Date: 04/25
Effective Date: 07/21

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 Employment Opportunity

Equal Opportunity Employer / Disability / Vet