Job detail

Research Associate

Cooper University Hospital

#FDA #Healthcare #Orthopedics #Medical Office #Quality Improvement #Clinical Research #Patient Recruitment #IRB #Clinical Innovations

Quick overview

Assists the Principal Investigator with IRB protocols, consent forms, and study budget development. Responsible for recruiting study participants and maintaining all required study documentation for the IRB and FDA.

Requirements summary

Requires 0-2 years of experience in a medical office environment and proficiency in Microsoft Office Suite. A bachelor's degree is preferred.

bachelor degreeQuality ImprovementMicrosoft ExcelMicrosoft WordMicrosoft OutlookMicrosoft PowerPointPatient RecruitmentMedical Office OperationsSource Document VerificationIRB Protocol PreparationStudy Budget Development

Job description

About Us At Cooper University Health Care, our commitment to providing extraordinary health care begins with our team.
Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols.
We have a commitment to our employees to provide competitive rates and compensation programs.
Cooper offers full and part-time employees a comprehensive benefits program, including health, dental, vision, life, disability, and retirement.
We also provide attractive working conditions and opportunities for career growth through professional development.Discover why Cooper University Health Care is the employer of choice in South Jersey.
Short Description Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, and development of study budget.
Completes and maintains all study documents as required and assists with the identification and recruitment of study participants.
Work as a team player with all involved in the research studies Assists the Principal Investigator and other members of the research team with the preparation of IRB protocols, consent forms, and development of the study budget.Assists in the identification and recruitment of study patients.
Assists in meeting with sponsors for study audits and source document verification.Assists in Quality Improvement activities.
Completes and maintains all study documents as required by the IRB, Cooper Health System, sponsor, and the FDA.
Works as a team player, cooperating and willing to assist coworkers and supervisors involved with the studies.
Performs all related duties or special projects as assigned/required.
Experience Required 0-2 Years Required Experience with word, excel, power point and outlook required.Experience in a medical office environment, handling multiple proj3ects and office operations required.
Education Requirements Bachelor Degree Preferred Salary Min ($) USD $23.00 Salary Max ($) USD $37.00

Research Associate

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