Research Data Coordinator II - Heme | Meyloid
Competitive
You'll complete your application on the employer's website.
Competitive
You'll complete your application on the employer's website.
Job type
Salary
Competitive
Location
Sector
Posted
30+ Days Ago
Moffitt Cancer Center is seeking a Research Data Coordinator II to support cancer research studies. The role autonomously reviews and synthesizes medical record information to extract protocol-specific trial data, manage data requirements across multiple research projects, resolve queries, and ensure compliance with good clinical practice and federal regulations.
Responsibilities
The Research Data Coordinator II (RDC II) autonomously reviews and synthesize information from medical records (clinic notes, pathology reports, radiology reports, patient questionnaires, etc.) to extract industry, cooperative, and investigator-initiated trial data as specified by assigned research protocols
The position is responsible for protocol specific data requirements for multiple research projects, while ensuring data requirements are in alignment with good clinical practice according to Federal regulations
The role will routinely handle complex tasks
It will determine methods and procedures related to data requirements, query resolution and data capture
The role collaborates with the study coordinator and monitors regarding the protocol requirements
This is a fully proficient role performing all RDC core support and additional responsibilities including higher patient volume and/or higher trial complexity
Workload is more complex and comprehensive than lower-level research data coordinators
The position assists less-experienced team members
Presents in department meetings as appropriate
Preferred
Previous experience doing this type of work in the oncology research setting
Through knowledge of EMR systems (e.g. Powerchart), clinical trial management systems (e.g. OnCore) and other data entry systems
Oncology research experience
EMR systems
PowerChart
Clinical trial management systems
OnCore
Data entry systems
Benefits
Virtual (Remote Eligible Position)
Opportunity for career growth within the Research Data Coordinator career path
Company
Comprehensive cancer hospital and research center
Tampa, Florida, USA
http://moffitt.org/
Founded in 1986
10001+ employees
Qualifications
High School Diploma/GED with three (3) three years of data management required
*In lieu of experience, an AA/AS degree plus one (1) year of clinical or research data management is acceptable
Must possess effective verbal and written communication skills as well as excellent interpersonal skills with staff and other health care professionals
Must have ability to prioritize and pace one's-self when working under the pressure of deadlines and work volume
Experienced in using automated data processing techniques, word processing software, experience using data base software programs required
Must be able to interpret all components of the medical record
Must be able to maintain confidentiality requirements as well as security of subject data
Excellent oral and written communication skills needed
Must be comfortable talking to physicians and other health care professionals
In this position, the role will work independently under limited supervision with some latitude for independent judgment. Normally receives little instruction on daily work, general instructions on newly introduced assignments
The Manager/Supervisor or Principal Investigator will provide more detailed instructions on new complex assignments where there is limited prior depth, or breadth of knowledge or working experience
Previous experience doing this type of work in the oncology research setting
Through knowledge of EMR systems (e.g. Powerchart), clinical trial management systems (e.g. OnCore) and other data entry systems
High School Diploma/GED with three (3) three years of data management required.
*In lieu of experience, an AA/AS degree plus one (1) year of clinical or research data management is acceptable.
Required skills
Clinical research data management, Medical record interpretation, Clinical trial data management, EMR systems (PowerChart), Clinical trial management systems (OnCore), Database software
Preferred skills
Written and verbal communication
Experience
3+ years
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