Clinical Research Coordinator

Florida Onc; Naples, Northern (FL, KY); Hybrid; USD 25,000 - 39,000; Full time

Job summary

American Oncology Network is seeking a Clinical Research Coordinator I (non-RN) in Florida to support the performance and ongoing management of multiple clinical trials under PI supervision.

Responsibilities include protocol coordination, data integrity, and regulatory compliance, with regular office hours and potential remote work as required. Prior research experience and strong communication are essential.

Qualifications

• High school education required; some college preferred.
• Prior research or related medical science experience.
• Ability to manage multiple trials and ensure regulatory compliance.
• Excellent communication and organizational skills.

Responsibilities

• Coordinate care for patients on clinical research protocols.
• Adhere to GCP/ICH-FDA guidelines and regulatory requirements.
• Assist with data collection, entry and reporting for trials under supervision.
• Prepare documents for monitoring visits and ensure protocol compliance.

Skills

Analysis & Critical Thinking

Interpersonal Effectiveness

Communication Skills

Customer Service

Self-Management

Education

High school diploma

Some college

Tools

MS Office

EMR

EDC

CTMS

Job description

Clinical Research Coordinator page is loaded## Clinical Research Coordinatorlocations: US-FL-Naplestime type: Full timeposted on: Posted 2 Days Agojob requisition id: JR7417**Location:**Florida Oncology and Hematology**Hiring Range:**$18.00 - $28.08# **Job Description Summary**Responsible 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 Areas****KPA 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 supervision* Conduct protocol feasibility assessments and complete feasibility/site assessment questionnaires* Identifies and explains inclusion/exclusion criteria and the process of subject identification, prescreening, screening and re-screening* Knowledge 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 protocol* Follows 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 supervision* Ensures 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 Integrity*** Follows 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 file* Comply 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 supervision* Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials* Prepare 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 leadership**KPA 3 - Research Financial Practices: Budget/Contract execution and practices research billing compliance*** Identifies elements of a study budget as it relates to execution of a protocol.# **Position Qualifications/Requirements****Education*** High school education required* Some college is preferred**Previous Experience*** Prior research or related medical science experience**Core Capabilities*** **Analysis & 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 Skills*** Proficiency in MS Office Word, Excel, Power Point, and Outlook required.* Prior experience with electronic medical records (EMR) is preferred* Prior experience with clinical trial data entry systems (EDC) preferred* Prior Clinical Trial Management Systems (CTMS) preferred.## **Travel**: 0%**Standard Core Workdays/Hours**: Monday to Friday 8:00 AM - 5:00 PM.######AONC**American Oncology Network**AON is an alliance of physicians and veteran healthcare leaders dedicated to ensuring the long-term success and viability of oncology diagnosis and treatment in community-based settings. It is the fastest growing national network of community oncology practices delivering local access to exceptional cancer care.AON serves its expanding network of partner practices by providing proven practice management expertise. Our employees across the country work together to empower physicians to make cancer care better. By driving integrated, collaborative care, we are proudly helping community oncologists deliver the highest quality care to every patient.Cancer touches everyone. Being able to make a difference in the lives of those fighting this disease is something our employees at AON cherish and never take for granted. A career in oncology offers all sorts of rewards. But working at AON offers employees more than most.* As a fast-growing national company, the opportunity to join a national workforce with flexible work options is available. We offer competitive compensation packages that include comprehensive health insurance with a robust provider network. Our 401k, which offers a 100% match and investment options, is available to full-time and part-time staff members, and we feature a generous Paid Time Off (PTO) program.* At AON, we offer you more than a job, we offer you a career. As a network of independent oncology practices working together as one, we host annual summits each year, providing our employees a chance to collaborate with AON peers from across the country. Promoting from within is a priority at AON, and we support our team members continued growth through professional development programs and tuition assistance.