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Job Posting Title:

Location:

Additional Posting Details:

Monday - Friday

8:00am - 5:00pm

Job Description:

Duties/Responsibilities

• Assist in preparation and maintenance of research and regulatory documents for Research Advisory Panel, Institutional Review Board, and other regulatory agencies

• Identify eligible patients and obtain informed consent

• Collect, validate, and enter data into research databases or spreadsheets

• Assist with the preparation and submission of abstracts, journal manuscripts and other presentations as needed

• Supervise summer students/interns and contribute to the training of Level I and new Level II Research Coordinators 

Required Skills/Abilities

• Bachelor’s Degree required; Master’s Degree preferred

• 3-5 years of experience in clinical research

• CCRP certification

• Must have proficient computer skills in a Windows environment; spreadsheet software knowledge a plus

• Ability to effectively communicate and collaborate with other health professionals as well as substantial interpersonal skills necessary to communicate with patients, their families, and the community.

• Critical thinking skills and time management skills are required; must have the ability to multi-task and work with minimal supervision

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