Research Study Coordinator

Clearview Cancer Institute•Huntsville, AL

16h•Onsite

About The Position

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.

Requirements

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
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.

Nice To Haves

BSN RN preferred.
GCP certification preferred.
OCN certification preferred.
At least (1) year research experience is preferred.

Responsibilities

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.