CASY-MSCCN Jobs

Title: Research Assistant

Location: Upper East Side

Org Unit: End of Life Research Center

Work Days:

Exemption Status: Non-Exempt

Salary Range: $22.03 - $25.99

*As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices

Position Summary

Under direction, provides research, data analysis and operational support to principal investigators and research coordinators for clinical research studies

Standard office work

Bachelor's degree is preferred.

Approximately one year of related experience.

Job Responsibilities

• Maintains a team-oriented approach, and possesses the ability to cultivate positive and collegial workplace relationships.

• High School Diploma

• Coordinates the recruitment and enrollment of study participants. Assesses patient eligibility for inclusion in clinical trials. Ensures proper consent protocols have been followed for study participation.

• Statistical and database management experience, including proficiency in SPSS and/or RedCap.

• Data Compilation

• Demonstrates integrity and ethics at all times.

• Assists with departmental mailings, including patient medical records. Ensures accuracy of recipient contact information and location for correct delivery.

• Previous clinical research experience is helpful.

• Statistical Analysis

• Understands the need to be responsible for our own outcomes, and takes pride in delivering the best possible work product.

• Conducts literature reviews and gains expert familiarity with protocols that will be used as templates.

• Knowledge of medical terminology is helpful.

• Oral/Written Communications

• Possesses the ability to facilitate the flow of information through effective written and oral communication.

• Assists in creation of study database.

• Analytical skills

• Possesses excellent work-related skills and the ability to apply them, while continually seeking ways to improve.

• Manages and enters collected data into study database.

• Approaches our job knowing that there are internal and external customers whose expectations we strive to exceed.

• Conducts qualitative coding and thematic analysis of study data.

• Appreciates and understands the connection between individual goals, departmental goals and the organizational mission.

• May perform statistical analysis of research data.

• Maintains a flexible and forward thinking approach to the way work is done.

• Assists in the preparation of materials, submissions and renewals to the Institutional Review Board (IRB) or IACUC.

• Assists faculty in the preparation of grant submissions and associated documentation, which may include just-in-time documents, progress reports, routing forms, abstracts and manuscripts.

• Performs other related duties as directed.

Education

• Maintains a team-oriented approach, and possesses the ability to cultivate positive and collegial workplace relationships.

• High School Diploma

• Coordinates the recruitment and enrollment of study participants. Assesses patient eligibility for inclusion in clinical trials. Ensures proper consent protocols have been followed for study participation.

• Statistical and database management experience, including proficiency in SPSS and/or RedCap.

• Data Compilation

• Demonstrates integrity and ethics at all times.

• Assists with departmental mailings, including patient medical records. Ensures accuracy of recipient contact information and location for correct delivery.

• Previous clinical research experience is helpful.

• Statistical Analysis

• Understands the need to be responsible for our own outcomes, and takes pride in delivering the best possible work product.

• Conducts literature reviews and gains expert familiarity with protocols that will be used as templates.

• Knowledge of medical terminology is helpful.

• Oral/Written Communications

• Possesses the ability to facilitate the flow of information through effective written and oral communication.

• Assists in creation of study database.

• Analytical skills

• Possesses excellent work-related skills and the ability to apply them, while continually seeking ways to improve.

• Manages and enters collected data into study database.

• Approaches our job knowing that there are internal and external customers whose expectations we strive to exceed.

• Conducts qualitative coding and thematic analysis of study data.

• Appreciates and understands the connection between individual goals, departmental goals and the organizational mission.

• May perform statistical analysis of research data.

• Maintains a flexible and forward thinking approach to the way work is done.

• Assists in the preparation of materials, submissions and renewals to the Institutional Review Board (IRB) or IACUC.

• Assists faculty in the preparation of grant submissions and associated documentation, which may include just-in-time documents, progress reports, routing forms, abstracts and manuscripts.

• Performs other related duties as directed.

Experience

Under direction, provides research, data analysis and operational support to principal investigators and research coordinators for clinical research studies

Standard office work

Bachelor's degree is preferred.

Approximately one year of related experience.

Knowledge, Skills and Abilities

• Maintains a team-oriented approach, and possesses the ability to cultivate positive and collegial workplace relationships.

• High School Diploma

• Coordinates the recruitment and enrollment of study participants. Assesses patient eligibility for inclusion in clinical trials. Ensures proper consent protocols have been followed for study participation.

• Statistical and database management experience, including proficiency in SPSS and/or RedCap.

• Data Compilation

• Demonstrates integrity and ethics at all times.

• Assists with departmental mailings, including patient medical records. Ensures accuracy of recipient contact information and location for correct delivery.

• Previous clinical research experience is helpful.

• Statistical Analysis

• Understands the need to be responsible for our own outcomes, and takes pride in delivering the best possible work product.

• Conducts literature reviews and gains expert familiarity with protocols that will be used as templates.

• Knowledge of medical terminology is helpful.

• Oral/Written Communications

• Possesses the ability to facilitate the flow of information through effective written and oral communication.

• Assists in creation of study database.

• Analytical skills

• Possesses excellent work-related skills and the ability to apply them, while continually seeking ways to improve.

• Manages and enters collected data into study database.

• Approaches our job knowing that there are internal and external customers whose expectations we strive to exceed.

• Conducts qualitative coding and thematic analysis of study data.

• Appreciates and understands the connection between individual goals, departmental goals and the organizational mission.

• May perform statistical analysis of research data.

• Maintains a flexible and forward thinking approach to the way work is done.

• Assists in the preparation of materials, submissions and renewals to the Institutional Review Board (IRB) or IACUC.

• Assists faculty in the preparation of grant submissions and associated documentation, which may include just-in-time documents, progress reports, routing forms, abstracts and manuscripts.

• Performs other related duties as directed.

Licenses and Certifications

• Maintains a team-oriented approach, and possesses the ability to cultivate positive and collegial workplace relationships.

• High School Diploma

• Coordinates the recruitment and enrollment of study participants. Assesses patient eligibility for inclusion in clinical trials. Ensures proper consent protocols have been followed for study participation.

• Statistical and database management experience, including proficiency in SPSS and/or RedCap.

• Data Compilation

• Demonstrates integrity and ethics at all times.

• Assists with departmental mailings, including patient medical records. Ensures accuracy of recipient contact information and location for correct delivery.

• Previous clinical research experience is helpful.

• Statistical Analysis

• Understands the need to be responsible for our own outcomes, and takes pride in delivering the best possible work product.

• Conducts literature reviews and gains expert familiarity with protocols that will be used as templates.

• Knowledge of medical terminology is helpful.

• Oral/Written Communications

• Possesses the ability to facilitate the flow of information through effective written and oral communication.

• Assists in creation of study database.

• Analytical skills

• Possesses excellent work-related skills and the ability to apply them, while continually seeking ways to improve.

• Manages and enters collected data into study database.

• Approaches our job knowing that there are internal and external customers whose expectations we strive to exceed.

• Conducts qualitative coding and thematic analysis of study data.

• Appreciates and understands the connection between individual goals, departmental goals and the organizational mission.

• May perform statistical analysis of research data.

• Maintains a flexible and forward thinking approach to the way work is done.

• Assists in the preparation of materials, submissions and renewals to the Institutional Review Board (IRB) or IACUC.

• Assists faculty in the preparation of grant submissions and associated documentation, which may include just-in-time documents, progress reports, routing forms, abstracts and manuscripts.

• Performs other related duties as directed.

Working Conditions/Physical Demands

Under direction, provides research, data analysis and operational support to principal investigators and research coordinators for clinical research studies

Standard office work

Bachelor's degree is preferred.

Approximately one year of related experience.

Weill Cornell Medicine is a comprehensive academic medical center that is committed to excellence in patient care, scientific discovery, and the education of future physicians and scientists in New York City and around the world. Our doctors and scientists - faculty from Weill Cornell Medical College, Weill Cornell Graduate School of Medical Sciences, and the Weill Cornell Physician Organization - are engaged in world-class clinical care and cutting-edge research that connect patients to the latest treatment innovations and prevention strategies. Located in the heart of the Upper East Side's scientific corridor, Weill Cornell Medicine's powerful network of collaborators extends to its parent university Cornell University; to Qatar, where an international campus offers a U.S. medical degree; and to programs in Tanzania, Haiti, Brazil, Austria and Turkey. Our medical practices serve communities throughout New York City, and our faculty provide comprehensive care at NewYork-Presbyterian Hospital/Weill Cornell Medical Center, NewYork-Presbyterian/Lower Manhattan Hospital, NewYork-Presbyterian Hospital/Brooklyn Methodist Hospital, NewYork-Presbyterian Hospital/Westchester Behavioral Health Center, and NewYork-Presbyterian/Queens. At Weill Cornell Medicine, we work together to treat each individual, not just their conditions or illnesses, as we strive to deliver the finest possible care for our patients - the center of everything we do. Weill Cornell Medicine is an Equal Employment Opportunity Employer. Weill Cornell Medicine provides equal employment opportunities to all qualified applicants without regard to race, sex, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, or genetic information.