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Full-time
bachelor degree
Posted 12d ago
~40 hrs/week
Responsibilities
The Research Study Coordinator manages the day-to-day planning, execution, and monitoring of oncology clinical research protocols to ensure trial integrity and patient safety. Responsibilities include patient recruitment, data collection, adverse event reporting, and the management of investigational products.
Requirements
Candidates must be a registered nurse (RN) in Alabama with at least one year of experience in oncology and infusion. Strong computer skills, proficiency in MS Office, and the ability to handle complex clinical trial protocols are required.
Full job description
Clearview Cancer Institute is north Alabama's leading cancer treatment facility. For over 30 years Clearview Cancer Institute has provided leading-edge treatment and compassionate care to those diagnosed with cancer or blood disorders. Clearview offers every service and amenity needed in an outpatient setting and our dedication to research and involvement in Phase I-IV clinical trials gives our patients the opportunity to receive potentially life-saving treatment options.
Why Join Us? We are looking for talented and highly-motivated individuals who demonstrate a natural desire to support the meaningful work of community oncologists and the patients we serve.
Job Description:
Job Purpose
A Research Study Coordinator is responsible for the day-to-day planning, execution, and monitoring of complex oncology clinical research protocols. This is done in a manner to assure trial integrity and patient safety.
Essential Job Functions
Consents and acknowledges personal data are provided to study sponsors, CROs, auditors, and authorities in accordance with reporting guidelines for clinical trials, ICH, and the Code of Federal Regulations.
Coordinates with research team, other CCI departments, trial sponsors, and patients to ensure protocol adherence
Manages data collection, source documentation, case report forms, and adverse event reporting
Performs patient recruitment, screening, enrollment, and follow-up in accordance with the trial's protocol
Maintains GCP (Good Clinical Practice) and IATA certifications as required to uphold FDA standards regarding clinical trials
Responsible for all aspects of managing and documenting Investigational Product (IP); including arrival, storage, tracking, and dispensation to research participants.
Coordinate and attend trial initiation visits and attend all protocol required meetings and trainings.
Coordinate patient care, safety, trial data collection, and quality with treating providers, PI, research staff, necessary CCI departments, and external providers
Perform consent process defined by ICH GCPs and CCI Research SOPs.
Directly interact with patients for clinical trial schedules, treatments, follow-up and study information.
Pre-screening of patients using available electronic platforms for possible inclusion in clinical trials.
Report SAEs according to protocol and SOPs.
Maintain patient privacy and confidentiality in accordance with applicable law.
Maintain study confidentiality.
Must have strong computer skills and working knowledge of MS Office Suite, cloud-based EMR systems, data capture systems, medical terminology, and oncology terminology.
Must be willing to learn and adapt to changing practices, systems, and requirements for efficient clinical management and clinical trial execution
Provide payment milestones per CTA in a timely manner.
Comply with CCI and departmental policies and procedures.
Duties as assigned for trials according to trial delegation logs (DOAs) for clinical trials at CCI.
Qualifications
Must have demonstrated proficiency with Microsoft 365.
Must have working knowledge of computer data management systems.
Must have interest in clinical research.
Must be detail-oriented with strong critical-thinking skills.
Must have excellent communication skills, both oral and written
Must work well independently and with diverse teams.
Must have the ability to handle multiple priorities in a fast-paced environment
Must have the ability to understand complex clinical trial protocols
Education/Experience
Must be registered nurse RN in good standing with the State of Alabama.
Must have at least (1) year infusion experience.
Must have at least (1) year oncology experience, preferred 2 years of oncology experience.
Must have at least (1) year EMR experience.
BSN RN preferred.
GCP certification preferred.
OCN certification preferred.
At least (1) year research experience is preferred.
Working conditions
This position works in the research department of a busy outpatient medical facility. Direct patient care is required.
Physical requirements
Must be able to safely move patients.
Must be able to lift and carry 30 pounds.
Must be comfortable standing and walking for long periods of time.
Must be willing to travel domestically up to 25% of the time.
Must have reliable transportation.
Direct reports
This position is not a supervisory position.
Related keywords
Research Study CoordinatorOncologyClinical TrialsPhase I-IVGCPIATAFDARNBSNOCNEMRPatient CareProtocol AdherenceInformed ConsentSAE ReportingInvestigational Product
Tennessee Oncology is one of the nation’s largest community-based cancer care specialists and home to one of the leading clinical trial networks in the country.
Established 1976 in Nashville, Tennessee Oncology’s mission remains unchanged: To provide access to high quality cancer care and the expertise of clinical research for all patients at convenient locations within their community and close to their home. To this day, our growing network of physicians and number of locations is based on this mission. In 2018, Tennessee Oncology joined OneOncology, a partnership of oncologists and industry leading experts driving the future of community-based cancer care in the United States, as a founding practice partner.
Physicians specializing in gynecologic oncology, palliative care, radiation oncology, and health psychology comprise our group.
Tennessee Oncology provides a full range of diagnostic services, including oncology specific expertise in PET/CT and laboratory services. Clinic locations provide on-site chemotherapy treatments so that patients receive care in their community and close to their home.
Our physicians utilize the latest in molecular diagnostics and profiling to choose treatments specific to the genetics of your cancer.
Oncology research is the largest area of new drug development. Self -administered medications, those taken by mouth or injected by the patient, comprise approximately 40% of these investigative medications. Tennessee Oncology’s in house pharmacy, Park Pharmacy, stocks oncology and hematology medications not readily available at community retail pharmacies. A URAC accredited Specialty Pharmacy, Park provides insurance and benefits investigation, prior authorization services for insurance coverage, co-pay assistance through manufacturer or foundation programs, extensive medication education, and access to a pharmacist 24 hours a day, 7 days a week.
Offices: 2004 Hayes St, Nashville, Tennessee 37203, US
How many Healthcare jobs are open in Huntsville, AL right now?
There are currently 1,105 open healthcare positions in Huntsville, AL listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Healthcare roles in Huntsville, AL?
Companies currently hiring include Huntsville Hospital, WellStone, Tennessee Oncology, Encompass Health, CVS Health, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Healthcare jobs in Huntsville, AL?
Yes — 29 of the 1105 open healthcare positions offer remote or hybrid work (12 remote, 17 hybrid).
How do I apply for Healthcare jobs in Huntsville, AL?
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