Sarah Cannon Development Innovations is a full service contract research organization ( CRO ) that is uniquely focused in oncology. Sarah Cannon Innovations offers strong scientific leadership, access to patients through Sarah Cannon Research Institute's Site Management Organization (SMO) and relationships with other clinical sites, and experience in drug development and delivery of clinical trials from First In Man through registration level studies, making us the partner of choice for oncology.
Our differentiator is strong operational delivery in partnership with our Site Management Organization and physician leaders to deliver your program efficiently.
Sarah Cannon Development Innovations works with Sarah Cannon Research Institute strategic and network sites throughout the United States, along with investigators at sites outside of the Sarah Cannon Research Institute network. This reach allows Sarah Cannon Development Innovations to offer sponsors access to a diverse and varied patient population, spanning multiple tumor types and disease stages. These relationships further enhance the depth and breadth of Sarah Cannon Development Innovations' therapeutic expertise, enabling it to provide focused, strategic operational support. This support ensures that clinical trials are conducted in a timely manner and reported with high quality, registration standard data.
Sarah Cannon, the global cancer enterprise of Hospital Corporation of America (HCA), offers integrated cancer services with convenient access to cutting edge therapies for those facing cancer in communities across the United States and United Kingdom.
Summary of Position:
This position is responsible for clinical data management of SCRI clinical trials. This includes all data management activities from protocol review to the final data deliverable to the sponsor. The Clinical Data Analyst supports data management project activities according to pre defined timelines and ensures timely completion of those projects. This position must clearly demonstrate the ability to manage multiple projects with different sponsors and timeline demands.
Duties and Responsibilities
Duties include but are not limited to:
Ensure quality and integrity of clinical data
Review clinical data as required by data cleaning plans and generate queries to investigator sites
Collaborate with investigator sites and CRAs to resolve data issues and ensure timely data entry and query resolution
Recommend corrective action for data handling issues
Perform reconciliation of non CRF data with CRF data
Drive problem solving with sites, sponsors, statisticians, project managers, physicians and other team members to ensure all data review issues are resolved. This includes identification of the problem, identifying the solution and coordinating the execution of the solutions
Responsible for ensuring adherence to the Data Management Plan for all data quality activities
Contribute to the establishment of study timelines and milestones
Report status of data and data issues to the project team. Escalate issues appropriately
Develop CRF Completion Guidelines and obtain appropriate approvals
Create and Maintain project documentation relevant to data management activities
Keep management abreast of issues and progress on all assigned projects
Keep Clinical Data Manager (CDM) informed of any data issues or cleaning status on all assigned projects
Collaborate with CDM on creating a manual review listing for assigned projects
Mentor and train new and/or junior data management staff as requested
Contributes to internal process development and improvement
Knowledge: A body of information needed to perform a tasks; May be obtained through education, training or experience
An understanding of scientific/research methods
Skills: The proficiency to perform a certain task
Excellent communication skills, oral, written and presentation
Excellent organizational skills
Excellent problem solving skills
Excel, MS Word
Proficiency in managing and organizing computer files
Abilities: An underlying, enduring trait useful for performing duties
Ability to manage multiple projects simultaneously
Strong attention to detail
Ability to concentrate for long periods of time
Ability to work independently to accomplish goals
Minimum Required: Bachelor's College Degree (4 year program)
Preferred: Bachelor's College Degree (4 year program)
1 3 years' experience working with detailed information
At least 1 year of professional experience in data analysis or data management
Experience working professionally in a healthcare organization
Clinical Trial experience in data management or trial management
**If interested in advancing your career with a growing leader in cancer research please apply today!
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