Clinical Research Associate

As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing:

 Performing monitoring visits according to plan, document actions and follow up on action plans
 Site feasibility visits incl. analysis of site logistics, site personnel performance/quality indicators and accountability for patient recruitment strategies
 Train and guide site staff in the protocol and trial procedures to minimize protocol deviations (PDs)
 Train site staff in safety information handling and systems
 Know and meet all local and company requirements with respect to safety reporting
 Proactive use of EDC and other data source systems for preparation and conduct of site visits as well as source data verification in collaboration with data management/logistics team
 Identify potential risks and proactively take action to prevent or mitigate
 Collaborate with Data Management/logistics in resolving queries
 Ensure data cleaning cycle timelines are met in accordance with the Data Flow Plan
 Manage trial product requirements, incl. temperature deviations and training of site staff
 Motivate and build strong relations with site personnel to ensure NN is their preferred clinical research partner
 Ensure collaboration with and deliverables from vendors locally, if applicable
 Collection and management of essential documents

You are:

 Primary point of contact between site staff and NN. Acts as ambassador for the company and contributes to making NN the preferred partner.
 Responsible for taking leadership of site management for the selection and initiation of sites as well as conduct and closing activities of the appointed studies in compliance with local regulations, ICH-GCP,
 NN procedures and protocol requirements to ensure data quality and study subject protection.
 Responsible for managing the site to meet patient recruitment rate and target.
 Delivers results that have direct impact on the successful completion of the clinical program.
 Coordinates with PM and communicates to them progress and critical issues that may impair trial progress.

Why ICON?

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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.

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.