Research Study Coordinator
About The Position
Rutgers, The State University of New Jersey is seeking a Research Study Coordinator for the Krieger Klein Alzheimer's Center within the Institute for Health, Health Care Policy and Aging Research. Among the key duties of the position are the following: Conducts human subjects research using appropriate interview techniques, including conducting informed consent processes, screening participants, completing assessments and evaluations. Maintains research study records, subject files, and databases, including providing overall study monitoring and protocol compliance per GCP guidelines, HIPAA, IRB and institutional and sponsor guidelines. Conducts literature reviews to support grant proposal development. Prepares and ships clinical specimens as required by the protocol. Attends continuing education and compliance training as necessary.
Requirements
- Bachelor's degree in a related field, or an equivalent combination of education and/or experience.
- A valid driver's license would be required for this position.
- Effective oral, written and interpersonal communication skills including the knowledge of proper business writing style and format.
- Strong interest and enthusiasm in helping achieve successful implementation of research and contributing to cutting-edge science.
- Phlebotomy experience or willingness to learn phlebotomy.
- Knowledge and skills using MS Office Suite and other standard office software, Web conferencing programs such as Zoom, and using collaborative documents and programs such as Google Docs.
- Clean Driving Record.
Nice To Haves
- Cultural and language competency and/or experience working with one or more of the underserved communities of NJ.
Responsibilities
- Conducts human subjects research using appropriate interview techniques, including conducting informed consent processes, screening participants, completing assessments and evaluations.
- Maintains research study records, subject files, and databases, including providing overall study monitoring and protocol compliance per GCP guidelines, HIPAA, IRB and institutional and sponsor guidelines.
- Conducts literature reviews to support grant proposal development.
- Prepares and ships clinical specimens as required by the protocol.
- Attends continuing education and compliance training as necessary.
Benefits
- Medical, prescription drug, and dental coverage
- Paid vacation, holidays, and various leave programs
- Competitive retirement benefits, including defined contribution plans and voluntary tax-deferred savings options
- Employee and dependent educational benefits (when applicable)
- Life insurance coverage
- Employee discount programs
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What This Job Offers
Job Type
Part-time
Career Level
Entry Level
Industry
Educational Services
Number of Employees
5,001-10,000 employees
