Clinical Research Coordinator Nurse II

Meharry Medical College; Vaughan; On-site; CAD 32,000 - 39,000; Full time

Job summary

A leading healthcare institution seeks a Clinical Research Coordinator Nurse II to oversee clinical research projects. This role involves managing compliance with regulations, coordinating participant activities, and supporting financial functions in research protocols. Ideal candidates will be licensed nurses with significant experience in patient care and clinical research.

Qualifications

• Registered Nurse license required.
• Minimum 60 months of experience in a patient care setting.
• Clinical research experience preferred.

Responsibilities

• Coordinate clinical research projects with oversight, ensuring compliance and quality.
• Assess eligibility of study subjects and maintain accurate records.
• Perform specific protocol procedures and manage related financial functions.

Skills

Clinical research practice

Computer proficiency

Judgment in evaluating information

Ability to enter results accurately

Ability to work under stress

Team orientation

Education

Licensed as a registered nurse in Tennessee

Graduated from an accredited nursing program

Job description

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The Clinical Research Coordinator II (CRC II) will be responsible for coordinating advanced clinical research projects proficiently with supervision. Functions independently, and is able to identify situations where additional support is necessary. Independently able to access regulations governing the protection of human subjects- IRB, FDA, OHRP, GCP / ICH and HIPAA guidelines and apply regulations in practice. The CRC II will assure that the integrity and quality of clinical research trials is maintained and the trials are conducted in accordance with all Meharry Medical College, IRB, and NIH policies and standard operating procedures. Responds to inquiries on study projects, ensures compliance of protocols and overall objectives, and performs study-related procedures of clinical research under the supervision of the Principal Investigators. The CRCII will assist with the operational and financial functions of the Center of Excellence for Clinical and Translational Research.

Daily Operations

• Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and nurses and travel to participant’s location for recruitment activities
• Maintain required records of study activity including case report forms, consenting research subjects, or regulatory forms.
• Performs standard accounting functions, monitors and reviews accounting and related system reports for accuracy and completeness; prepares and reviews budget, revenue, expenses, invoices, and other accounting documents; Responsible for collecting and documentation of monies collected in clinical research. Responsible for managing accounts receivable and accounts payable in clinical research; Assist with reviews, analyzes and negotiates all clinical research budgets and contracts with sponsors under the direction of the Principal Investigator / Associate Director
• Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms. Direct the requisition, collection, Processing of samples, labeling, storage, or shipment of specimens.
• Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
• Schedules subjects for appointments and procedures as required by study protocols. Inform patients or caregivers about study aspects and outcomes to be expected.
• Assists with preparing IRB submissions, protocol revisions, and renewals as needed, and maintain copies of all IRB communications delegated by the Principal Investigator.
• Performs other related duties as assigned.

Required Skills

• Must possess a good working knowledge of basic clinical research practice.
• Must be proficient with personal computer.
• Ability to utilize keen judgment in evaluating information.
• Ability to numerically and accurately enter and calculate test results in an electronic database.
• Ability to work in a stressful environment.
• Must be team oriented.

Required Education And Experience

• Graduated from an accredited discipline specific program and licensed as a registered nurse in the state of Tennessee. 60 months experience in a patient care setting required (Experience as a travel nurse or clinical research experience preferred).

Seniority level

Seniority level

Entry level

Employment type

Employment type

Full-time

Job function

Job function

Research, Analyst, and Information Technology

Higher Education

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