DescriptionThe Clinical Research Coordinator (CRC) is an entry human subjects researcher responsible for assisting the lab leadership (including but not limited to CRC I) in clinical research studies.
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.
- Assists in the activities related to clinical research including but not limited to: obtaining informed consent screening participants for eligibility registering patients with sponsoring agencies administering bilingual 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.
- Assists in the collection analysis and review of experimental data for publication and presentation.
- Assist in maintaining source documents and subject files in accordance with Mount Sinai policies and procedures.
- Ensures accurate confidential and complete compilation of data.
- May secure and ship clinical specimens as required by the protocol.
- Assist in other related administrative duties as needed.
Qualifications- Bachelors degree is required
- Being able to speak write type and read proficient English Mandarin and Cantonese.
Required Experience:
IC
DescriptionThe Clinical Research Coordinator (CRC) is an entry human subjects researcher responsible for assisting the lab leadership (including but not limited to CRC I) in clinical research studies.ResponsibilitiesConducts routine and standardized human subjects research using appropriate research...
DescriptionThe Clinical Research Coordinator (CRC) is an entry human subjects researcher responsible for assisting the lab leadership (including but not limited to CRC I) in clinical research studies.
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.
- Assists in the activities related to clinical research including but not limited to: obtaining informed consent screening participants for eligibility registering patients with sponsoring agencies administering bilingual 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.
- Assists in the collection analysis and review of experimental data for publication and presentation.
- Assist in maintaining source documents and subject files in accordance with Mount Sinai policies and procedures.
- Ensures accurate confidential and complete compilation of data.
- May secure and ship clinical specimens as required by the protocol.
- Assist in other related administrative duties as needed.
Qualifications- Bachelors degree is required
- Being able to speak write type and read proficient English Mandarin and Cantonese.
Required Experience:
IC
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