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 an experience professional with a passion for clinical contract development and negotiationYou are organized, but flexible and adaptable to unexpected changesYou can easily envision the bigger picture, without losing sight of the day-to-day tasksYou can provide excellent leadership to not only your project teams, but also to clientsYou are excited and enthusiasticYou motivate your teams to do great work and collaborate easily with your clientsMost 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?
Strong communication (written and verbal) skills to be able to interact with internal vertex groups as well as external groups
Strong attention to detail
Ability to understand the contract and budget process at a high level
What do you need to have?
Routing the clinical trial agreement (cta) for signature, either via paper if wet ink required or through docusign
Coding of the budgets
Qc of the ctas to ensure all signatures are completed, execution date is present and protocol number is consistent throughout
Distribution of the cta to appropriate stakeholders
Filing in an electronic repository and entering medidata based on information from the cta and budget
Assisting the sc leads with metric reports and review
Other duties as applicable
Qualifications
Minimum of 1- 2 years of related experience preferred
Bachelors degree required
Experience with pc-windows, word processing, and electronic spreadsheets required.
Knowledge of ich and local regulatory authority drug research and development regulations required.
Clinical trials support or pharmaceutical industry experience 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.
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