Data Manager Remote
Data Manager Remote
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Job Description
All fulltime university staff are eligible for VCUs robust benefits package that includes: comprehensive health benefits paid annual and holiday leave granted up front generous tuition benefit retirement planning and savings options taxdeferred annuity and cash match programs employee discounts wellbeing resources abundant opportunities for career development and advancement and more. Learn more about VCUs benefits here.
Please note VCU is not able to provide current or ongoing visa sponsorship for this position.
Benefits At a Glance
- 28 Vacation Days 12 State Holidays and 4 Days to volunteer;
- Continuing education for undergraduate and graduate tuition for a maximum of 6 credits per semester;
- Professional development opportunities encouraged and offered for employees as part of annual career development e.g. certifications seminars courses annual conferences mentorship;
- Medical Dental and Vision Health Benefits to meet the needs of employees and their eligible family members from the Commonwealth of Virginia as well as optional FSA;
- Participation in the Virginia Retirement System (VRS) and other retirement saving options;
- Parental and Caregiver Leave Short Term Disability (STD) Disability Insurance Voluntary Long Term Care Insurance and Employee Assistance Program.
Massey Comprehensive Cancer Center
Mission: To reduce the state cancer burden for all Virginians by addressing the confluence between biological social and policy drivers through highimpact cuttingedge research; personcentered care across the continuum from prevention through survivorship; community integration; and training the next generation of communitycentric researchers and healthcare professionals
Vision: To be a premier communityfocused cancer center leading the nation in cancer health equity research and ensuring optimal health outcomes for all
Position Primary Purpose and General Responsibilities
The Massey Comprehensive Cancer Center (MCCC) Biostatistics Shared Resource (BSSR) seeks to hire a data management and reporting specialist to support clinical cancer research serving as an administrative liaison of data between the Clinical Trials Office (CTO) and the BSSR. The CTO includes a wide spectrum of oncology clinical studies and trials as well as clinical cancer researchers the clinical research office and fellow biostatisticians. Scientists strictly follow Good Clinical Practices (GCP) and all current laws regulations guidance policies and procedures developed by the Institutional Review Board (IRB) Code of Federal Regulations (CFR) and all federal state and local regulatory entities. Responsibilities of the Data Manager may be independent or as a member of a team. They work under general supervision resolving routinetocomplex issues independently and referring more complex issues to an upperlevel manager. This individual will report to the director of the BSSR but will work closely with key personnel within the CTO including the CTO director to ensure database development is in compliance with Common Data Elements (CDE).
The Data Manager will involve highly collaborative interactions with MCCC staff and investigators working alongside other staff to ensure quality control on various projects and attend core/project meetings. In addition to the responsibilities listed below other job responsibilities may be assigned with emphasis on:
1. Data capture and management for oncology clinical trials 50. Work with the Clinical Trials Office personnel to design and create databases for clinical studies and trials.
a. Develop and maintain REDCap databases.
2. Report generation for clinical trials 25. Help support ontrial monitoring by planning and creating regular reports on accrual data quality safety and (in some cases) efficacy. Oversee development and delivery of tables and reports for reporting for all trials.
a. Write modify maintain and validate computer programs for project reports.
b. Review and update statistical analysis plans to ensure accuracy.
c. Run systematic reports for clinical trials.
3. Create analysis data sets for clinical and translational studies 25. Work with biostatistical teams to organize trial and study data into analyzable formats provide basic summaries Tables and Figures conduct basic biostatistical analyses (ex. correlative studies) and assist with manuscript writing and preparation.
a. Develop analysis datasets using data from electronic data capture systems and registry data systems.
Minimum Qualifications
- Masters degree (MS ScM MPH etc. in Biostatistics Statistics Data Science or a related field or equivalent combination of education experience and training;
- 2 years experience with data management and statistical programming using R SAS and/or SQL;
- 2 years experience with electronic data capture (EDC) systems particularly REDCap;
- 2 years experience with clinical trial data structures research methodologies and/or regulatory compliance;
- Intermediate proficiency with Microsoft Excel Word Access and Outlook with the ability to adapt to a range of database applications.
Candidates whose resumes highlight the following previous experience will be prioritized:
- Demonstrated experience working in and fostering an environment of respect professionalism and civility with a population of faculty staff and students from various backgrounds and experiences or a commitment to do so as a staff member at VCU;
- Intermediate proficiency with data entry and word processing skills with the ability to analyze and interpret information effectively;
- Intermediate organizational abilities and a keen eye for detail to ensure accuracy and efficiency in all tasks;
- Clear and professional written and verbal communication skills with the ability to interact effectively with colleagues and stakeholders;
- Interpersonal skills capable of building relationships and collaborating with team members at all levels to gather information and support compliance efforts;
- Problemsolving and organizational aptitude with the ability to manage multiple tasks and meet deadlines in a dynamic environment.
Please note VCU is not able to provide current or ongoing visa sponsorship for this position.
Preferred Qualifications
- Doctoral degree or equivalent combination of education experience and training;
- 2 years experience with oncology clinical trials or biomedical research data management;
- 2 years experience with clinical trials management systems (CTMS) such as OnCore;
- Prior exposure to reporting and FDA data submission requirements;
- Advanced proficiency with Microsoft Excel Word Access and Outlook with the ability to adapt to a range of database applications;
- Past productivity as documented by publications.
Please let us know if you were referred by a current Massey employee to ensure we honor our commitment to the Employee Referral Program.
Required Experience:
Manager
Employment Type
Full Time
