Clinical System Designer -Patient Platform designs

Clinical System Designer - Patient Platform designs

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 System Designer -Patient Platform designs

Home or office-based in Poland

The Clinical System Designer uses technical, industrial, and interpersonal skills, with some support from project team leads and their people leader, to interpret clinical protocols and customer requirements in order to create ICON Patient Platform designs and non-Patient Platform component specifications to meet the needs of the customer and the clinical trial. 

What You Will Be Doing:

• Knowledge in identifying bugs or configuration issues

• Understanding of helpdesk systems and support triage process

• Experience working in highly regulated systems and environments

• Good functional knowledge of at least one clinical data management system and CRF design tool/eCOA platform and design tool
•Ability to plan and design Patient Platform components directly from interpretation of low to medium complexity clinical trial protocols.
Business Expertise:
• Acts as first point of contact during study build for assigned projects for design related questions by the project team.
• Read, ensure understanding and adhere to the study protocol, contract and scope of work for all task during set-up, maintenance and close-out of the study.
• Tracks and keeps functional management and those responsible for project management informed of any issues that might affect project target dates, scope or budget and escalates potential problems effectively and in a timely manner
• With support, consolidates and completes the high-level system requirements documents and facilitates their review.
• Assumes responsibility for copying and modifying eDiaries/eCOAs from standard libraries and other studies.
• Performs quality control peer reviews of database related specifications as needed and records comments appropriately.
• Lead specification review meetings
• Obtains required approvals for the release of system components to the live/production environment.
• Maintain and track meeting minutes, issues and decisions logs, and escalations where appropriate
• May take part in study kick off (internal and external) meeting as appropriate
•With support from other project team leads, assist in assessing impacts of post-production database related changes and compiling the change management documentation for review by project team leads.
• Other responsibilities may be assigned as required

Your Profile:

Experience in working within the Clinical Trial Industry

Familiarity with Clinical Systems

Experience in planning and designing Patient Platform components directly from interpretation of low to medium complexity clinical trial protocols

Leadership:
• Ability and willingness to assist team members.
• Embrace and contribute to a culture of process improvement with a focus on streamlining processes and adding value to the business and client needs.
• Travel (approximately 10 %) domestic and/or international

Problem Solving:
•Problems are varied and nonroutine. Uses previous experience to identify most appropriate solution.

Impact:

• Acts with urgency, able to prioritize items based on importance

• Contributes to the achievement of goals through personal effort and influence over others. Impact is focused on the achievement of short- to medium term goals.

Interpersonal Skills:
• Good written and oral communication and presentation skills.
• Good inter/cross-team communication skills.

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.

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 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