DescriptionThe Clinical Research Coordinator Part-time performs all the regular duties of a Clinical Research Coordinator but due to abbreviated hours doesntqualify for exemption. This is an hourly position which is eligible for overtime only intended to be used for part-time Clinical Research Coordinatorassists in the daily activities of clinical research studies obtains informed consent; collects maintains and organizes study information. Assists in preparing grant applications and documents (for e.g. Institutional Review Board Grants and Contracts Office).
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.
Qualifications- Bachelors degree in science or related field preferred or a combination of relevant research experience and education.
Non-Bargaining Unit 857 - Rehabilitation and Human Performance - ISM Icahn School of Medicine
Required Experience:
IC
DescriptionThe Clinical Research Coordinator Part-time performs all the regular duties of a Clinical Research Coordinator but due to abbreviated hours doesntqualify for exemption. This is an hourly position which is eligible for overtime only intended to be used for part-time Clinical Research Coor...
DescriptionThe Clinical Research Coordinator Part-time performs all the regular duties of a Clinical Research Coordinator but due to abbreviated hours doesntqualify for exemption. This is an hourly position which is eligible for overtime only intended to be used for part-time Clinical Research Coordinatorassists in the daily activities of clinical research studies obtains informed consent; collects maintains and organizes study information. Assists in preparing grant applications and documents (for e.g. Institutional Review Board Grants and Contracts Office).
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.
Qualifications- Bachelors degree in science or related field preferred or a combination of relevant research experience and education.
Non-Bargaining Unit 857 - Rehabilitation and Human Performance - ISM Icahn School of Medicine
Required Experience:
IC
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