Senior Clinical System Designer

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From 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 success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

The Role:

The Clinical System Designer uses technical, industrial, and interpersonal skills to create case report forms (CRFs) for trials.

• Lead and serve as main point of contact relevant to the Clinical Systems group. Directly engages with client and internal cross-functional teams.
• Creates case report forms (CRFs) from the study protocol
• Creates specifications for dynamic and edit checks
• Organizes, creates, and oversees the administration of training and mentoring for junior levels.
• Helps prepare materials and participate in industry meetings as a representative of ICON.
• Assists in the development of materials for the bid defense process and client demonstrations.
• Creates and maintains libraries for use in designing, developing, and testing all system components for a trial.
• Provides support and review for the re-use of library items.

To be successful in the role, you will have:

• Bachelor’s degree in a technological or clinical field required.
• Minimum of 5 years of clinical design experience required.
• Must have experience in building EDC studies. Medidata Rave / Veeva EDC preferred. Rave builder certification a plus.
• Experience performing post production changes in EDC platforms desired.
• Experience with integrations with IXRS desired.
• Must have prior experience building from the protocol. Must be able to read and understand protocol, and develop new CRFs with minimal support.
• Must be comfortable interfacing directly with clients and internal cross-functional teams (Lead Data Managers, Developers).

General:

To qualify for a role located in the U.S., applicants must be legally authorized to work in the United States and should not (now or in the future) require sponsorship for employment work visa status. 

Benefits of Working in ICON:
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.

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 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.

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, 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 through the form below.