Senior Cdc

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.

We have an incredible opportunity for a **Senior Clinical Data Coordinator** to join ICON’s Full Service Clinical Data Science team.

**LOCATIONS**:

- Mexico City (office-based with remote flexibility)
- Colombia (home-based OR office-based)

**OVERVIEW OF THE ROLE**:
The Senior Clinical Data Coordinator supports and executes the data review activities, including data validation and analytics, that contribute to delivery of clinical data that meets agreed upon data integrity standards. They will act as the Data Review Team lead for one or more projects and act as Subject Matter Expert (SME) for various technologies or procedures within the scope of role.
- Support activities related to development of the Clinical Data Management System as needed
- Detect risks and signals in the data using quality indicators
- Accountable for the development of the CRF Completion Guidelines and supporting/reviewing other Clinical Data Science documents
- Perform root cause analysis of detected data issues
- Ensure study and task metrics are tracked and reported to Clinical Data Science Lead, project team, and functional management
- Manages third party data reconciliation process
- Collaborate with cross-functional and global groups

**TO BE SUCCESSFUL, YOU WILL NEED**:

- 3+ years of clinical data management experience in a clinical research organization or pharmaceutical company
- Basic knowledge of the drug development process including risk-based monitoring principles
- Experience working on multiple projects simultaneously
- Data Analytic and Data Validation experience
- Strong knowledge of at least 1 Clinical Data Management System (Medidata RAVE, InForm, Veeva, etc.)
- Excellent written and oral communication skills
- Bachelor’s degree or local equivalent
- _ Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above. All employees must read, write, and speak fluent English and host country language._

**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.