DescriptionThe Alzheimers Disease research Center (ADRC) is looking for a full-time bilingual (Spanish and English speaking) clinical research coordinator whose responsibilities will include completing study activities related to the NIH funded ADRC UDS observational study. These duties include but are not limited to attending outreach events recruiting participants and scheduling and completing study visits per protocol.
Responsibilities- Collects and records study data. Inputs all information into database.
- Attending outreach events and recruiting scheduling and completing study visits
- 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.
Qualifications- Bachelors or Masters degree in Science or closely related field.
- No experience required. One year of research experience preferred.
- Bilingual Spanish/English speaking
Required Experience:
IC
DescriptionThe Alzheimers Disease research Center (ADRC) is looking for a full-time bilingual (Spanish and English speaking) clinical research coordinator whose responsibilities will include completing study activities related to the NIH funded ADRC UDS observational study. These duties include but ...
DescriptionThe Alzheimers Disease research Center (ADRC) is looking for a full-time bilingual (Spanish and English speaking) clinical research coordinator whose responsibilities will include completing study activities related to the NIH funded ADRC UDS observational study. These duties include but are not limited to attending outreach events recruiting participants and scheduling and completing study visits per protocol.
Responsibilities- Collects and records study data. Inputs all information into database.
- Attending outreach events and recruiting scheduling and completing study visits
- 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.
Qualifications- Bachelors or Masters degree in Science or closely related field.
- No experience required. One year of research experience preferred.
- Bilingual Spanish/English speaking
Required Experience:
IC
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