Biological Sciences Division at the University of Chicago
Senior Clinical Research Data Manager
Biological Sciences Division at the University of Chicago, Chicago, Illinois, United States, 60290
Overview
The Senior Clinical Research Data Manager will perform a variety of data management duties of a complex and technical nature in support of clinical research studies conducted by principal investigators (PIs) for the clinical research program to ensure adherence to protocols and quality of information received. Base pay range $60,000.00/yr - $75,000.00/yr Department BSD MED - Hematology and Oncology - Clinical Research Data Managers - Cluster 5 Job Summary The Senior Clinical Research Data Manager will perform a variety of data management duties of a complex and technical nature in support of clinical research studies conducted by principal investigators (PIs) for the clinical research program to ensure adherence to protocols and quality of information received. Responsibilities
Maintains a close, collaborative working relationship with the PIs in your department to effectively manage research studies, with the department, administrative team, and department staff. Builds and maintains effective relationships with key study personnel, clinical resources and colleagues. Oversees the data management activities of a specific work unit as the data management expert. Responsible for all data management aspects of clinical studies and efficiently performs all data management activities within an assigned study or studies. Provides data management expertise to the team in identifying opportunities for improvement. Ensures validity of research results through timely, accurate, and complete data submission, query resolution, and reporting of deviations. May delegate tasks to team members within the study program. Demonstrates proficiency in the use of clinical and research-related computer programs. Ensures that relevant data from the source document are abstracted and recorded in the clinical trial case report forms and that every data point can be verified within the source document. Utilizes analytical thinking, attention to detail, and problem-solving skills. Facilitates communication between the site and study sponsor, CRO, and/or regulators, and exhibits teamwork skills necessary for managing the data collection and reporting process. Will train other data managers within the unit. S Solves a range of straightforward problems relating to the administration of the compliance, financial and other related aspects of a clinical study. Accountable for all data management tasks in support of moderate to high-complexity clinical research studies, which may include a mix of industry, investigator-initiated trials (IITs), and National Cancer Trial Network (NCTN) trials, under limited supervision and while maintaining a high degree of confidentiality. Primary study assignments are considered a higher risk in terms of impact on the reputation and integrity of cancer centers and are generally provided less oversight from external clinical trial monitoring. Coordinates document collection and review in collaboration with the principal investigator (PI). Performs other related work as needed. Education & Experience
Minimum Qualifications Minimum requirements include a college or university degree in related field. Work Experience Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline. Qualifications
Preferred Qualifications Bachelor's degree. Progressively responsible relevant clinical research experience. Proven excellence in data management and related skills. Perform data monitoring, query generation and query resolution. Perform research data management with minimal supervision. Knowledge of Microsoft Word, Excel and Adobe Acrobat. Knowledge of medical and/or clinical trial terminology. Train junior data managers. Experience troubleshooting clinical trials and identifying appropriate interventions. Knowledge in relevant scientific field.
Technical Skills & Competencies
Strong analytical skills; attention to detail. Proficiency with clinical data management and data-related software. Work collaboratively with divisional research offices and maintain confidentiality of clinical data and client data. Adaptability to changing assignments; ability to work independently and as part of a team. Excellence in multi-tasking. Application Documents
Resume/CV (required) Cover Letter (required) When applying, the document(s) must be uploaded via the My Experience page, in the section titled Application Documents of the application. Job Details
Job Family: Research Role Impact: Individual Contributor Scheduled Weekly Hours: 37.5 Pay Rate Type: Salary FLSA Status: Exempt Pay Range: $60,000.00 - $75,000.00 Benefits Eligible: Yes The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, or expression, national or ethnic origin, age, disability status, or other protected classes. Reasonable accommodations will be provided for applicants with a need. Background checks apply to offers of employment. Posting statements and safety information are provided for applicants and may include links to the university safety report and related resources.
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The Senior Clinical Research Data Manager will perform a variety of data management duties of a complex and technical nature in support of clinical research studies conducted by principal investigators (PIs) for the clinical research program to ensure adherence to protocols and quality of information received. Base pay range $60,000.00/yr - $75,000.00/yr Department BSD MED - Hematology and Oncology - Clinical Research Data Managers - Cluster 5 Job Summary The Senior Clinical Research Data Manager will perform a variety of data management duties of a complex and technical nature in support of clinical research studies conducted by principal investigators (PIs) for the clinical research program to ensure adherence to protocols and quality of information received. Responsibilities
Maintains a close, collaborative working relationship with the PIs in your department to effectively manage research studies, with the department, administrative team, and department staff. Builds and maintains effective relationships with key study personnel, clinical resources and colleagues. Oversees the data management activities of a specific work unit as the data management expert. Responsible for all data management aspects of clinical studies and efficiently performs all data management activities within an assigned study or studies. Provides data management expertise to the team in identifying opportunities for improvement. Ensures validity of research results through timely, accurate, and complete data submission, query resolution, and reporting of deviations. May delegate tasks to team members within the study program. Demonstrates proficiency in the use of clinical and research-related computer programs. Ensures that relevant data from the source document are abstracted and recorded in the clinical trial case report forms and that every data point can be verified within the source document. Utilizes analytical thinking, attention to detail, and problem-solving skills. Facilitates communication between the site and study sponsor, CRO, and/or regulators, and exhibits teamwork skills necessary for managing the data collection and reporting process. Will train other data managers within the unit. S Solves a range of straightforward problems relating to the administration of the compliance, financial and other related aspects of a clinical study. Accountable for all data management tasks in support of moderate to high-complexity clinical research studies, which may include a mix of industry, investigator-initiated trials (IITs), and National Cancer Trial Network (NCTN) trials, under limited supervision and while maintaining a high degree of confidentiality. Primary study assignments are considered a higher risk in terms of impact on the reputation and integrity of cancer centers and are generally provided less oversight from external clinical trial monitoring. Coordinates document collection and review in collaboration with the principal investigator (PI). Performs other related work as needed. Education & Experience
Minimum Qualifications Minimum requirements include a college or university degree in related field. Work Experience Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline. Qualifications
Preferred Qualifications Bachelor's degree. Progressively responsible relevant clinical research experience. Proven excellence in data management and related skills. Perform data monitoring, query generation and query resolution. Perform research data management with minimal supervision. Knowledge of Microsoft Word, Excel and Adobe Acrobat. Knowledge of medical and/or clinical trial terminology. Train junior data managers. Experience troubleshooting clinical trials and identifying appropriate interventions. Knowledge in relevant scientific field.
Technical Skills & Competencies
Strong analytical skills; attention to detail. Proficiency with clinical data management and data-related software. Work collaboratively with divisional research offices and maintain confidentiality of clinical data and client data. Adaptability to changing assignments; ability to work independently and as part of a team. Excellence in multi-tasking. Application Documents
Resume/CV (required) Cover Letter (required) When applying, the document(s) must be uploaded via the My Experience page, in the section titled Application Documents of the application. Job Details
Job Family: Research Role Impact: Individual Contributor Scheduled Weekly Hours: 37.5 Pay Rate Type: Salary FLSA Status: Exempt Pay Range: $60,000.00 - $75,000.00 Benefits Eligible: Yes The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, or expression, national or ethnic origin, age, disability status, or other protected classes. Reasonable accommodations will be provided for applicants with a need. Background checks apply to offers of employment. Posting statements and safety information are provided for applicants and may include links to the university safety report and related resources.
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