Research Data Coordinator
Highlands Oncology Group
Administration
Springdale, AR, USA
Posted 6+ months ago
Research Data Coordinator
Highlands Oncology Group
3.3 out of 5
Springdale, AR 72762
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Find out how your skills align with the job descriptionCertifications
Skills
Education
Location
Springdale, AR 72762
Full job description
Highlands Oncology Group is dedicated to providing the highest quality of innovative care delivered with compassion and precision. It is only by the efforts of our determined and dedicated team of nearly 700 amazing people that we are able to accomplish that goal. Join a team that is honored to be an important part of the journey our patients are on as they battle cancer.
The Research Data Coordinator is responsible for data collection, consistent with Good Clinical Practice Guidelines, the Highlands Oncology Group policies and procedures, and sponsor requirements within the assigned setting.
Communication Skills
- Demonstrates a high level of professionalism and responsiveness when interacting with internal and external customers.
- Advises supervisor or other appropriate individuals of problems and concerns.
- Collaborates effectively with physicians, nurses, and ancillary departments.
- Communicates routinely with supervisor/liaison regarding program status.
- Demonstrates effective oral and written communication skills.
- Attends research department meetings when held.
Accountability/Dependability
- Maintains subject/sponsor confidentiality.
- Promptly reports to work at designated times.
- Maintains good attendance and no unexcused absences.
- Follows up on issues as appropriate.
- Supports and adheres to organizational decisions, policies, and procedures.
- Willingly accepts assignments and completes them in a timely manner.
Organizational Skills
- Maintains organized files and office space.
- Effectively sets priorities.
- Demonstrates flexibility in schedule to accommodate workload.
- Submits routine reports on or before due date.
Professional Growth
- Demonstrates professionalism in appearance/dress code consistent with policy.
- Seeks to increase skills through self-directed learning activities.
- Willing to take continuing education courses as appropriate.
- Acts as team member both corporately and within the individual setting.
Physical Requirements
- May be asked to lift up to 25 pounds.
- Will require extensive sitting and standing.
Education Required
- High school graduate or higher education.
Experience Required
- Possess excellent organizational skills.
- Proficient in Microsoft Office Applications, including MS Word and Outlook.
- Demonstrates effective oral and written communication skills.
Preferred Qualifications
- Healthcare and clinical research experience
- Clinical Research Professional (CCRP) certification within three years of hire.
- Takes initiative to reliably complete tasks independently.
- Experience with electronic medical records.
Job Duties and Responsibilities
- Maintains documentation of source data.
- Prepares/maintains subject research information.
- Notifies Principal Investigator, Clinical Research Coordinator, and sponsor of patient issues.
- Works with investigators, nurses, and Clinical Research Coordinator to identify/document toxicity, adverse events, etc.
- Acts as a resource to hospital and clinic personnel/physicians regarding research activity.
- Works closely with the Clinical Research Coordinators to collect/maintain accurate source documentation.
- Prepares/maintains protocol files accurately and in a timely fashion.
- Submits subject data that is accurate, complete, timely, neat, and in accordance with protocol parameters.
- Works with multiple databases.
- Works with Clinical Research Coordinators to deidentify Research Imaging Scans and transmit to
- Outside Imaging Vendors.
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