Project Analyst I

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.

With our patients at the center 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 Project Analyst can be based anywhere in the United States

Home or Office based

• The Project Analyst I (POA) is a key member of the operational study team.
• The primary responsibility of this role is to ensure high quality metrics and performance data for the programs assigned.
• The POA will support traditional RWE studies which include registries, observational studies, pragmatic trials, and other post approval study designs. The POA will also support studies conducted by ICO Medical Device and Diagnostics group, Epidemiology, Health Economics and Outcomes Research, and consultancy programs.
• The POA will work with project teams, the data analytics group, data management and other cross departmental services to obtain necessary data elements to populate trackers and analytic reports.
• POAs will participate in routine project review meetings and re-baselining meetings as needed for the studies they are assigned.
• POAs will work on a variety of studies and will rotate their workload based upon the priorities of the department.

Additionally, as part of the team, the POA will:

• Recognize, exemplify and adhere to ICON's values which center on our commitment to People, Clients and Performance
• Actively support the growth and integration of assigned functional team or service area.
• Adhere to project communication plan ensuring communication needs are met
• Work collaboratively with project team's project to ensure timelines and data integrity maintained.
• Anticipate and respond to project needs with limited or no guidance.
• Responsible for accurate tracking and regular upkeep of operational data on projects.
• Identify risks with assigned tasks and projects and effectively execute strategies to minimize those risks.
• Support project meetings and the resolution of issues, project recaps and corrective/preventative action plans.
  Such other duties and tasks as allocated at the reasonable discretion of management.
• Travel (approximately 5%) domestic and/or international

Requirements

• 4+ years of Clinical Research experience, or relevant pharmaceutical industry experience
• Ability to interpret data (analytical skills), and use this analytical outcome to help drive the data requirements of the team, and organization, through established processes
• Excellent communication in English (written and oral), organizational, and time management skills. Ability to build relationships with all levels of stakeholders.
• Proficient working knowledge and regular usage of MS office package. Experience with Clinical Operational systems is a plus.
• Ability to work both independently and as part of a team

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.

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