Mount Sinai Health System
The 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 women’s 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
Bachelor’s degree in science or closely related field preferred
Master’s degree in science or closely related field preferred
1 year in research environment preferredExperience 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
Equal Opportunity Employer The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law. We are deeply committed to fostering an environment where all faculty, staff, students, trainees, patients, visitors, and the communities we serve feel respected and supported. Our goal is to create a healthcare and learning institution that actively works to remove barriers, address challenges, and promote fairness in all aspects of our organization.
Compensation The Mount Sinai Health System (MSHS) provides salary ranges that comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for the role is $17.3644 - $21.5971 Hourly. Actual salaries depend on a variety of factors, including experience, education, and operational need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.
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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
Bachelor’s degree in science or closely related field preferred
Master’s degree in science or closely related field preferred
1 year in research environment preferredExperience 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
Equal Opportunity Employer The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law. We are deeply committed to fostering an environment where all faculty, staff, students, trainees, patients, visitors, and the communities we serve feel respected and supported. Our goal is to create a healthcare and learning institution that actively works to remove barriers, address challenges, and promote fairness in all aspects of our organization.
Compensation The Mount Sinai Health System (MSHS) provides salary ranges that comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for the role is $17.3644 - $21.5971 Hourly. Actual salaries depend on a variety of factors, including experience, education, and operational need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.
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