Clinical Research Assistant I
- Conduct protocol management for an assigned set of multiple research protocols.
- Maintain current and accurate protocol documentation and notify investigators of pertinent protocol changes.
- Ensure participants are appropriately registered and maintain documentation of participant registration.
- Compile and submit data on appropriate forms according to protocol requirements.
- Ensure protocol compliance through intense monitoring of specific study requirements and schedule protocol-related activities.
- Play an active role in the recruitment of participants for the study.
- Assist in training and mentoring new clinical research staff members.
- Perform protocol-specific clinical duties as required by the research study.
- Perform data management and data analyses as required by the research study.
- Establish and maintain interpersonal relationships with participants, visitors, and other hospital personnel while ensuring the confidentiality of participant information.
- Collect and deliver specimens for analysis using appropriate equipment for collecting and handling specimens, ensure proper labeling, and obtain pertinent clinical and protocol information on request forms.
- Develop and maintain knowledge of various aspects of processing specimens, with particular attention to safety practices.
- Identify and communicate important protocol and data management issues or problem areas to the supervisor.
- Associate's Degree.
- Experience may substitute for minimum education requirements.
- Read, identify and extract pertinent data from medical records.
- Ability to read, write and comprehend medical terminology.
- Medical Record, Health Information Systems, or related health field.
- Bachelor's degree.
- Bilingual/Biliterate English/Spanish for regular written and verbal communications in Spanish with research participants and collaborating investigators.
- Experience with Progeny preferred.
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