CLINICAL RESEARCH COORDINATOR - ONCOLOGY

Automatic Data Processing, Inc.; Maumee (OH); On-site; USD 30,000 - 40,000; Full time

Job summary

Taylor Cancer Research Center in Maumee, OH is seeking a Clinical Research Coordinator for oncology. This full-time role ensures the integrity and quality of clinical trials, in compliance with IRB approvals, SOPs, and applicable regulations.

You will assist investigators in coordinating patient participation and study activities. Responsibilities include screening and enrolling patients, performing required tests, administering investigational medications when applicable, educating

Qualifications

• 2–4 years in medical practice with oncology/acute care preferred.
• Knowledge of clinical care coordination and patient management.
• Attention to detail in collecting and analyzing data for trials.
• Strong verbal and written communication; familiarity with regulatory requirements.

Responsibilities

• Ensure protocol compliance and accurate documentation at each visit.
• Recruit and screen study participants for eligibility.
• Perform clinical tests and administer investigational medications as applicable.
• Educate patients on medication use and disease treatment and follow up.
• Maintain regulatory documents and data in CTMS and sponsor systems.
• Collaborate with sponsors, monitors, investigators, and study teams.
• Maintain confidentiality and safety in all trial activities and report issues as needed.

Skills

Oncology experience

Clinical coordination

Regulatory compliance

Education

Bachelor's degree

Job description

CLINICAL RESEARCH COORDINATOR - ONCOLOGY

Taylor Cancer Research Center Full Time Salary 30-40 Maumee, OH, US

2 days ago Requisition ID: 5072

General Summary:

The Clinical Research Coordinator will ensure the integrity and quality of clinical trials are maintained and conducted in accordance w/ federal, state, and local regulations, Institutional Review Board (IRB) approvals, and with program Standard Operating Procedures. This position is also responsible to ensure completeness, accuracy and compliance with each protocol and to assist Investigators of clinical studies in coordinating and facilitating the activities of study patients.

• Ensures compliance with each study’s protocol by providing thorough review and documentation at each subject study visit.
• Participates in recruitment and selection of study participants by interviewing and documenting medical history to determine compliance with eligibility requirements. Interfaces with study participants, to support efforts to determine eligibility and consenting requirements according to protocol.
• Performs medical or research required tests, including, but not limited to, vital signs, imaging studies, specimen collection and processing, and electrocardiograms.
• Administers investigational medications, as applicable, and performs patient assessments during clinic visits to determine presence of side effects; notifies Principal Investigator of findings/issues.
• Provides patient education and medical information to study participants to ensure understanding of proper medication dosage, administration, and disease treatment.
• Documents medical data in patient chart to capture protocol requirement.
• Ensures site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities.
• Develops accurate source materials and ensures compliance.
• Provides accurate and timely data collection, documentation, entry, and reporting in both sponsor and TCCC electronic medical record, databases / Clinical Trial Management System (CTMS), etc.
• Supports clinical research operations team in the maintenance of regulatory documents in accordance with SOP and applicable regulations.
• Communicates and collaborates specific study requirements to the research team, including internal and external parties, sponsor, monitors, Investigators, and study patients.
• Participates with the research operations team to identify and prioritize the development of systems and infrastructure to maintain research quality and compliance.
• Maintains good rapport and cooperative relationships. Approaches conflict in a constructive manner. Helps to identify problems, offer solutions, and participate in their resolution.
• Maintains the confidentiality of information acquired pertaining to patient, physicians, employees, and visitors. Discusses patient and hospital information only among appropriate personnel.
• Assumes responsibility for performance of job duties in the safest possible manner, to assure personal safety and that of coworkers, and to report all preventable hazards and unsafe practices immediately to management.
• Actively demonstrates the organization's mission and core values and conducts oneself at all times in a manner consistent with these values.
• Knows and adheres to all laws and regulations pertaining to patient health, safety and medical information.

Knowledge, Skills & Abilities:

Required:

• 2-4 years experience in medical practice with prior experience in oncology and/or an acute care setting, preferred.
• Proven knowledge in patient treatment and coordination of clinical care.
• Attention to detail required in collecting and analyzing data.
• Strong verbal and written communication skills for interacting with patients and reporting research findings.
• DOT/IATA Training (must be obtained within 30 days of hire).
• Certification in Human Subjects Protection, Good Clinical Practices (must be obtained within 30 days of hire)
• Adherence to all Toledo Clinic policies and procedures.

Education:

• Bachelor’s degree and/or equivalent experience

Preferred:

• Experience conducting clinical research, including enrolling patients in research studies, implementing research protocols and presenting findings.