United BioSource Corporation.

Nurse Clinician RN [Cross Functional]

Overland Park, US
18 Jul 2019
17 Aug 2019
Clinical Research
Full Time
Contract Type
Experience Level
Experienced (non-manager)
Brief Description:
The Nurse Clinician - RN is responsible for reviewing escalated clinical criteria reviews for providers, members and patient client advocates within the Prior Authorization/Utilization Management department. Identify and track trends for analytics reporting to ensure clinical criteria program integrity. Maintain a professional and ethical behavior at all times as outlined by the Nurse Practice Act and applicable company policies.

Specific job duties:
• Perform escalated clinical review and analysis of clinical program descriptions for clinical and criteria integrity.
• Maintains contact database and responds to member and physician inquiries regarding clinical programs. Makes recommendations regarding escalation of issues, and follows through with escalation process.
• Acts as liaison between clients, patients and patient care advocates to provide guidance on clinical criteria.
• Performs initial clinical review and analysis of prior authorization cases based on state regulations.
• Special projects/assignments as needed.

• Nursing degree
• 2-5 years' experience in a clinical setting
• Registered Nursing Licensure
• General PC knowledge including Microsoft Office, Internet and email
• Previous clinical criteria review experience preferred;
• Active professional affiliations and/or national certification in related clinical specialty preferred;
• Able to work flexible work schedule


United BioSource Corporation (UBC) is a leading provider of pharmaceutical support services, partnering with life science companies to make medicine and medical products safer and more accessible. Our services support the full lifecycle of medicine and medical products, including development, commercialization, and long-term value and safety.

While UBC offers employment within Patient Support, Nursing, Pharmacy and Corporate, two main focus areas for the company are Clinical Development & Research and Safety & Risk Management. Members of the Clinical Development and Research teams help evaluate study protocol, target study population, recruit physicians and patients, and collect, clean, validate and report data. As a result, sponsors are able to submit findings to regulatory authorities or make a no-go decision in a timely and clear-cut manner. Additionally, our Safety and Risk Management teams develop, deliver, and report evidence to reinforce safe and appropriate product use.

Through our Patient Access services, we help patients begin therapy quickly and remain on therapy, building strong relationships with patients to ensure optimal care.
You can find out more by visiting


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