DescriptionThe Clinical Research Assistant I assists in the daily activities of clinical research studies collects maintains and organizes study information. Assists in preparing grant applications and documents (for e.g. Institutional Review Board (IRB) Grants and Contracts Office (GCO)) and provides clerical support to Clinical Research Coordinators and others in assigned area. This role will include work on research projects in the Department of Obstetrics Gynecology and Reproductive Sciences. The CRA I will assist with projects related to womens health and clinical research methodology.
Responsibilities- 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
- Collects and records study data. Inputs all information into database
- 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.
- Assists in the preparation for monitoring visits
- Performs other related duties
Qualifications- Associates Degree in Science or closely related field preferred or HS/GED plus two years of related experience
- Bachelors degree in science or closely related field preferred
- Masters degree in science or closely related field preferred
- 1 year in research environment preferred
- Experience with IRB/GCO submissions the informed consent process study administration data collection and organization
- Excellent written and oral communication skills
- Excellent time management skills
- Exceptional attention to detail and accuracy
- Experience with Microsoft Office Suite required
- Preference for experience with R/SAS/SPSS Randomization and Trial Supply Management systems Electronic Data Capture systems and EPIC
DescriptionThe Clinical Research Assistant I assists in the daily activities of clinical research studies collects maintains and organizes study information. Assists in preparing grant applications and documents (for e.g. Institutional Review Board (IRB) Grants and Contracts Office (GCO)) and provid...
DescriptionThe Clinical Research Assistant I assists in the daily activities of clinical research studies collects maintains and organizes study information. Assists in preparing grant applications and documents (for e.g. Institutional Review Board (IRB) Grants and Contracts Office (GCO)) and provides clerical support to Clinical Research Coordinators and others in assigned area. This role will include work on research projects in the Department of Obstetrics Gynecology and Reproductive Sciences. The CRA I will assist with projects related to womens health and clinical research methodology.
Responsibilities- 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
- Collects and records study data. Inputs all information into database
- 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.
- Assists in the preparation for monitoring visits
- Performs other related duties
Qualifications- Associates Degree in Science or closely related field preferred or HS/GED plus two years of related experience
- Bachelors degree in science or closely related field preferred
- Masters degree in science or closely related field preferred
- 1 year in research environment preferred
- Experience with IRB/GCO submissions the informed consent process study administration data collection and organization
- Excellent written and oral communication skills
- Excellent time management skills
- Exceptional attention to detail and accuracy
- Experience with Microsoft Office Suite required
- Preference for experience with R/SAS/SPSS Randomization and Trial Supply Management systems Electronic Data Capture systems and EPIC
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