Clinical Research Coordinator

American Oncology Network; Naples (FL); On-site; USD 25,000 - 39,000; Full time

Job summary

The American Oncology Network is seeking a Clinical Research Coordinator I (non-RN) to oversee the execution and ongoing management of multiple clinical trials in a fast-paced, multi-site environment. You will coordinate patient care on protocols, ensure regulatory compliance, and support data integrity while working under physician supervision.

Key duties include protocol feasibility, patient screening, adverse event reporting, and collaboration with the sponsor, IRB, and study team.

Qualifications

• High school education required; some college preferred.
• Prior research or related medical science experience.
• Proficiency in MS Office; EMR/EDC/CTMS experience encouraged.
• Strong communication and ability to work remotely as required.

Responsibilities

• Coordinate care for patients on clinical research protocols per GCP/ICH guidelines.
• Identify inclusion/exclusion criteria and conduct prescreening and screening tasks.
• Review diagnostic tests and informed consent documentation.
• Document adverse events and report to sponsor/IRB as needed.
• Maintain regulatory compliance and data integrity across studies.
• Assist with budgeting, contracts, and study-related financial practices.

Skills

Analytical thinking

Interpersonal skills

Communication

Customer service

Self-management

Education

High school diploma

Some college

Tools

MS Office

EMR

EDC

CTMS

Job description

Location:Florida Oncology and HematologyHiring Range:$18.00 - $28.08Job Description SummaryResponsible for the performance of the research study under the medical supervision of the Principal Investigator. The Clinical Research Coordinator I (non-RN) is responsible for the overall successful implementation and ongoing management of the research studies. Ability to perform basics tasks and exhibit the knowledge of key aspects of clinical research at an essential or foundational levelPrimary responsibility includes study designs with entry-level complexity (phase 4, observational/registry trial design) and associated study procedures. Administratively and clinically manage an average 5 clinical trials open to accrual annually and/or active (on study treatment) patient volume 2-10 annually.Demonstrates working knowledge of all facets of role, relevant regulations, and organizational and departmental policies and procedures. Performs other duties and projects as assigned. Performs all duties in accordance with regulatory requirements and organizational policies and procedures.Primary Key Performance AreasKPA 1 – Protocol Comprehension and Implementation: Coordination of care for patients on clinical research protocols in accordance with GCP, ICH/FDA guidelines and requirements.Identify and explain key protocol elements and perform study tasks under direct supervisionConduct protocol feasibility assessments and complete feasibility/site assessment questionnairesIdentifies and explains inclusion/exclusion criteria and the process of subject identification, prescreening, screening and re-screeningKnowledge of the required elements of an informed consent form and the essential elements of the informed consent process.Review of diagnostic tests and related documentation required per protocolFollows process for capturing, assessing, determining causal relationship of adverse events to the investigational product, investigator oversight, reporting and following up on adverse events. Document different types of adverse events under direct supervisionEnsures proper storage, dispensing, handling and destruction processes for investigational products.Follows process for handling investigational products that have been compromised.KPA 2 – Regulatory and Data IntegrityFollows Institutional Review Board (IRB) / Independent Ethics Committee (IEC) review, approval and reporting requirements for the site. Maintains site credentials and ensures updated GCP, licenses remain on fileComply with reporting of safety related subject discontinuation and safety concerns (AE, SAE or AE of Interest) to the sponsor and IRB/IEC.Collect, record and report accurate data and demonstrate per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy under direct supervisionEnsure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trialsPrepare documents for monitoring visits under direct supervision. Review visit monitoring follow-up reports / letters and perform requested activities.Escalates issues of protocol non-compliance to study PI and research department leadershipKPA 3 – Research Financial Practices: Budget/Contract execution and practices research billing complianceIdentifies elements of a study budget as it relates to execution of a protocol.Position Qualifications/RequirementsEducationHigh school education requiredSome college is preferredPrevious ExperiencePrior research or related medical science experienceCore CapabilitiesAnalysis & Critical Thinking: Critical thinking skills including solid problem solving, analysis, decision-making, planning, time management and organizational skills. Must be detailed oriented with the ability to exercise independent judgment.Interpersonal Effectiveness: Developed interpersonal skills, emotional intelligence, diplomacy, tact, conflict management, delegation skills, and diversity awareness. Ability to work effectively with sensitive and confidential material and sometimes emotionally charged matters.Communication Skills: Good command of the English language. Second language is an asset but not required. Effective communication skills (oral, written, presentation), is an active listener, and effectively provides balanced feedback.Customer Service & Organizational Awareness: Strong customer focus. Ability to build an engaging culture of quality, performance effectiveness and operational excellence through best practices, strong business and political acumen, collaboration and partnerships, as well as a positive employee, physician and community relations.Self-Management: Effectively manages own time, conflicting priorities, self, stress, and professional development. Self-motivated and self-starter with ability work independently with limited supervision. Ability to work remotely effectively as required.Must be able to work effectively in a fast-paced, multi-site environment with demonstrated ability to juggle competing priorities and demands from a variety of stakeholders and sites.Computer SkillsProficiency in MS Office Word, Excel, Power Point, and Outlook required.Prior experience with electronic medical records (EMR) is preferredPrior experience with clinical trial data entry systems (EDC) preferredPrior Clinical Trial Management Systems (CTMS) preferred.Travel: 0%Standard Core Workdays/Hours: Monday to Friday 8:00 AM – 5:00 PM.#AONC#LI-ONSITE