Clinical trial research assistants will generally assist the Biopharma study team with the preparation, distribution, handling, filing, logging, and archiving of clinical documentation. The research assistant is a key support role to ensure the most effective and efficient conduct of clinical research studies by providing administrative and project tracking support. Additionally, research assistants should be or become capable of assisting with subject identification by becoming knowledgeable of protocols and maintaining a thorough understanding of GCP standards.

Job Responsibilities:

o Answer incoming calls

o Data Entry

o Chart Screening

o Schedule visits for subjects

o Patient outreach/communication for research

o Transportation scheduling as applicable

o Front desk duties as applicable

o Review of study protocols for understanding of criteria for designated studies

o Participate in the staff meetings as applicable

o Daily maintenance of CTMS and other applications as assigned

o Be under supervision of Team lead and upper management

o To follow any other verbal or written instructions given to you by supervisors

Experience Required:

o Minimum 1-2 years of medical terminology

o Medical Assistants encouraged to apply

o Professional phone communication and customer service

o Microsoft Office Suite experience is a must

o Computer savvy

o Data Entry—Attention to Detail

o Familiarity with research/clinical trials preferred

o Ability to read and comprehend protocols and other medical data

o Phlebotomy experience/certification is a plus

This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. Travel is primarily local, although some out-of-the-area travel may be expected.

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Research Assistant