Clinical Research Regulatory Coordinator Jobs in Arkansas

Assists SSU staff with the active project management of ongoing contract issues; performs follow-up on all outstanding contract issues.

Associate’s Degree or equivalent combination of education and training preferred.

Good organizational skills and good attention to detail, with proven ability to handle multiple tasks effectively.

Quality-driven in all managed activities.

Strong computer skills, including Word, Excel, PowerPoint, Publisher.

Assists with quality control processes and translation processes related to submissions, contracts and essential documents.

What is a nice to have (but not required) regarding skills, requirements, experience, education, or certification?

Required Skill 5: Experience with using clinical trial management systems

What years of experience, education, and/or certification is required?

Required Skill 1: Clinical Research Experience – could be in various roles (study coordinator, regulatory, compliance, safety, etc.)

What are the top 5 skills/requirements this person is required have?

Required Skill 3: Good communication

Experience using standard word processing and data management software programs, including Word and Excel, in order to develop and prepare reports.

Experience creating Informed Consent Documents that comply with HRPP/ IRB policies and procedures, FDA regulations, and sponsor requirements.

Experience with editing, including summarizing information into concise and condense documents.

Knowledge of oncology and hematology.

Experience working with FDA regulations, NCI policies and procedures, and Good Clinical Practice guidelines for the conduct of clinical research.

Working knowledge of Human Research Protections Program (HRPP/IRB) policies and Procedures.