RN Research Coord

Clinical Trial Coordinator

In coordination and collaboration with principal investigators, this job evaluates, initiates and maintains all activities related to the conduct of clinical trials in assigned area(s) of responsibility. Communicates effectively with external funding agencies, sponsors, departments, and patients to assure understanding of the requirements of conducting and participating in clinical trials. Organizes and manages all documentation and regulatory submissions as required by the sponsor of the trial, regulatory agencies, research division / Occupational Health and Safety (OHS) policy and company patient care requirements. Provides patient care and assessment as determined necessary by the clinical trial in coordination with other care providers.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and / or ability required. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential duties.

This job description is a summary of the primary duties and responsibilities of the job and position. It is not intended to be a comprehensive or all-inclusive listing of duties and responsibilities. Contents are subject to change at the company's discretion.

Education

Required - Registered nurse diploma.

Preferred - Bachelor's degree in nursing.

Work Experience

Required - 2 years of clinical experience.

Preferred - 3 years of experience in area of assigned clinical specialty, clinical research and managing patient databases.

Certifications

Required - Current registered nurse license in state of practice.

Basic Life Support (BLS) from the American Heart Association.

Knowledge Skills and Abilities (KSAs)

• Knowledge of medical and scientific terminology.
• Proficiency in using computers, software, and web-based applications.
• Effective verbal and written communication skills and the ability to present information clearly and professionally to varying levels of individuals throughout the patient care process.
• Excellent organizational, time management and prioritization skills and ability to pay close attention to detail.
• Critical thinking skills to process trial evaluation and submission, particularly the development of study related budgets, contracts and patient consent documents.
• Analytical skills and ability to interpret data.
• Ability to be self-directed.
• Ability to work a flexible work schedule (e.g. 24 / 7, weekend, holiday, on call availability) and travel throughout and between facilities.

Job Duties

The above statements describe the general nature and level of work only. They are not an exhaustive list of all required responsibilities, duties, and skills. Other duties may be added, or this description amended at any time.

Remains knowledgeable on current federal, state and local laws, accreditation standards or regulatory agency requirements that apply to the assigned area of responsibility and ensures compliance with all such laws, regulations and standards.

This employer maintains and complies with its Compliance & Privacy Program and Standards of Conduct, including the immediate reporting of any known or suspected unethical or questionable behaviors or conduct; patient / employee safety, patient privacy, and / or other compliance-related concerns.

The employer is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.