Clinical Nurse Reviewer I- IDEA

ICON; Raleigh (NC); Remote; USD 70,000 - 90,000; Full time

Job summary

ICON, a leading healthcare intelligence organization, seeks a Clinical Nurse Reviewer. This role entails the coordination and review of clinical trial documentation, requiring a Nursing Registration and solid experience in the clinical field. Join ICON to contribute to innovative clinical developments, offering competitive salary and comprehensive benefits.

Benefits

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Qualifications

• Two or more years of relevant work experience in drug development or clinical industry required.
• Adherence to Good Clinical Practices and FDA regulations.
• Experience with the MedDRA dictionary preferred.

Responsibilities

• Support Project Manager in coordination and receipt of clinical trial documents.
• Construct adjudication dossiers for physician review.
• Manage case-related information and ensure quality of submissions.

Skills

Critical thinking

Data Management

Communication

Organizational skills

Education

Nursing Registration

Tools

eCRFs

Microsoft Office Applications

Job description

Clinical Nurse Reviewer- IDEA

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

Clinical Nurse Reviewer

Location: Home-based

The Clinical Nurse Reviewer I provides support to the Project Manager in both coordination and receipt of clinical trial endpoint supporting source documents. This person is responsible for clinical content review of the endpoint source documentation for adjudication by the Endpoint adjudication committee.

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. This individual will manage activities relating to the collection, processing, analysis and follow-up of dossiers provided to Clinical Events Committees for marketed products and investigational compounds being studied in Endpoint Driven trials.

What you will be doing

·Ensures timely collection of documents and components of Adjudication Packages for Clinical Endpoint Committees to allow quality and complete adjudication of potential clinical endpoints occurring in clinical trials. Collect, QC and ensure that the package content is medically complete and appropriate to allow physician adjudicators the ability to apply objective endpoint definitions to each case presented to them.

·Must have knowledge of and adherence to all applicable aspects of Good Clinical Practices, Federal Regulations, International standards and company SOPs is required.

·Will construct medically complete and logical adjudication dossiers for presentation to physician adjudicators. Also responses to queries from Physician adjudicators, Clinical Site Personnel, Company Personnel as it relates to collection of dossier components.

·Will be responsible for, in collaboration with project management, generating status and progress reports for committees and tracking performance and quality among adjudicators. They will also work with Project Management and Clinical Operations to generate all necessary committee documentation, preparing periodic reports and reviews of certain cases, identify potential sources of un-blinding, extract Endpoint/AE data from various source documents and spontaneous sources.

·Manages case-related information including interpretation of medical conditions, lab results, and procedures as well as compile complete narrative summaries and ensure proper coding (MedDRA) into the Clinical Endpoint Committee database.

Your Profile:

• Nursing Registration is required along with two or more years of relevant work experience in drug development or clinical industry.
• Excellent critical thinking skills.
• Data Management experience is a plus.
• Experience working with FDA regulations and reporting requirements and experience working with the MedDRA dictionary is preferred.
• Experience working with electronic data (eCRFs), Microsoft Office Applications and other electronic data capture and transfer methods is highly desirable.
• Excellent verbal and written communication skills. Must be detailed oriented and possess excellent organizational skills.
• Willingness to travel 10%.

#LI-HH1

#LI-remote

What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply