DescriptionThe Clinical Research Coordinator I (CRC I) will be expected to lead and independently complete daily activities of clinical research studies as determined by the PI and other leadership in the lab. The CRC I will work closely with the lab leadership to report project updates and next steps.
Responsibilities- Conducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project under direct supervision of the PI and other leadership in the lab.
- Collects and records study data. Inputs all information into database.
- Activities related to clinical research including but not limited to: obtaining informed consent screening participants for eligibility registering patients with sponsoring agencies administering neuropsychological testing and questionnaires and answering telephone calls. Home visits and travel within the surrounding community/out-of-state will be required and communicated on a needs basis.
- Preparing grant applications IRB/GCO for submission and filings.
- Maintains source documents and participant files in accordance with hospital procedures. Ensures accurate and complete compilation of participant data through chart reviews.
- Secures delivers and ships clinical specimens as required by the protocol.
- Performs other administrative related duties as needed which may also include but is not limited to the training and supervision of CRCs and volunteers.
Qualifications- Bachelors or Masters degree in Science or closely related field.
- Prior work/internship experience in hospital/clinic/research setting
Note: Prior human subjects research experience is a plus - Being able to speak write type and read proficient English Mandarin and Cantonese.
Required Experience:
IC
DescriptionThe Clinical Research Coordinator I (CRC I) will be expected to lead and independently complete daily activities of clinical research studies as determined by the PI and other leadership in the lab. The CRC I will work closely with the lab leadership to report project updates and next ste...
DescriptionThe Clinical Research Coordinator I (CRC I) will be expected to lead and independently complete daily activities of clinical research studies as determined by the PI and other leadership in the lab. The CRC I will work closely with the lab leadership to report project updates and next steps.
Responsibilities- Conducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project under direct supervision of the PI and other leadership in the lab.
- Collects and records study data. Inputs all information into database.
- Activities related to clinical research including but not limited to: obtaining informed consent screening participants for eligibility registering patients with sponsoring agencies administering neuropsychological testing and questionnaires and answering telephone calls. Home visits and travel within the surrounding community/out-of-state will be required and communicated on a needs basis.
- Preparing grant applications IRB/GCO for submission and filings.
- Maintains source documents and participant files in accordance with hospital procedures. Ensures accurate and complete compilation of participant data through chart reviews.
- Secures delivers and ships clinical specimens as required by the protocol.
- Performs other administrative related duties as needed which may also include but is not limited to the training and supervision of CRCs and volunteers.
Qualifications- Bachelors or Masters degree in Science or closely related field.
- Prior work/internship experience in hospital/clinic/research setting
Note: Prior human subjects research experience is a plus - Being able to speak write type and read proficient English Mandarin and Cantonese.
Required Experience:
IC
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