Roles & Responsibilities:
- Collects and records study data. Inputs all information into database
- Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements
- Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires
- Assists in preparing grant applications, IRB/GCO for submission and filings
- Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews
- Secures, delivers and ships clinical specimens as required by the protocol
- Prepares for monitoring visits
- Performs other related duties
Requirements:
- Education: Bachelor's or Master's degree in Science or closely related field
- Experience: 1-2 years prior research experience
- Excellent written and oral communication skills
- Exceptional attention to detail and accuracy
More information and application are available here.
