Icon plc is a world-leading healthcare intelligence and clinical research organisationFrom molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our successIcon people have a mission to succeed and a passion that ensures what we do, we do well.
Who are you? you are a forward thinkerYou are an innovator that refuses to settleYou want to push the boundaries and change not just what it means to be a clinical trial associate, you want to change the futureYou want to learn from the best, grow your knowledge and your skill set, and you want to build your career hereYou want to use the latest technology and tools in the industry to push the momentum of an already growing company forwardYou want to find a balance that still lets you be, well, youMost of all, you want to do it in a place where you’re more than an employee numberA place you love working.
Still here? goodBecause if this is you, we’d really like to meet you.
Responsibilities
What will you be doing?
As a clinical trial associate , you will assists the clinical project managers in the conduct of trials and may be responsible for managing startup activities, vendor communication or other project activities as assignedHe/she performs work within established protocols under general supervision.
Assists with preparation of all external and internal documentation, for assigned trials, to ensure such documentation is completed in accordance with gcp regulatory requirements and is consistent with the study protocol, under close supervision
Assists clinical project manager in site management activities which could include review of monitoring report, tracking of site visits, communication with monitors and sites, and other activities as assigned
Maintains and tracks revisions to all documentation for accuracy, including patient informed consent forms and case report forms
Assists the clinical project manager in ensuring compliance with clinical study protocol and provides timely updates to assigned clinical project manager to confirm compliance
Organizes and prepares study files related to study tracking and reporting and submits them to the trial master file within established guidelines
May participate in the training of cro teams, investigators and staff as needed regarding assigned logistics of the clinical trial
Tracks delivery and receipt of required supplies and materials to study sites and provides regular status updates
May mentor more junior clinical operations staff or participate in the on boarding of new personnel
Performs other duties as assigned
Qualifications
What do you need to have?
Education: undergraduate degree or its international equivalent in clinical, science, or health related field from an accredited institution or a
Licensed healthcare professional
Skills:
2+ years of related experience
Read, write, and speak fluent english; fluent in host country language required
Benefits of working in icon:
Our success depends on the knowledge, capabilities and quality of our peopleThat’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.
At 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 programsIn 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.
Icon, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassmentAll 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.
Options
Apply Now onlineapply share sorry the share function is not working properly at this momentPlease refresh the page and try again laterShare on your newsfeed
Connect with us!
