Senior Clinical Data Coordinator
- Mexico City
- Clinical Data Management
- ICON Full Service & Corporate Support
- Remote or Office
About the role
Senior Clinical Data Coordinator - Mexico City (Hybrid)
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.
We have an incredible opportunity for a Senior Clinical Data Coordinator to join ICON’s Full-Service IOD Clinical Data Science team. The Senior CDC 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.
Locations: Mexico City (office-based an average of 3 days per week)
What you will be doing:
- 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
Your profile:
- 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.)
- Strong knowledge of computerized information systems and standard application software (Windows, MS Office)
- 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.
* Please submit all applications in English
#LI-Hybrid
#LI-TP1
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.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 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
Senior Talent Acquisition Business Partner
- Full Service Division
Explore more about ICON
Day in the life
Teaser label
A Day In The LifeContent type
BlogsPublish date
04/21/2023
Summary
From Clinical Trial Assistant to Clinical Operations Manager, Adrienne Purdy shares her journey. I have been at ICON since 2013 and I have been growing my career here from the ground up. I star
by
Adrienne Purdy
Teaser label
Our PeopleContent type
BlogsPublish date
12/22/2022
Summary
If there's one thing that the pandemic made clear, it was that clinical research was an essential part of the global recovery and protecting us from future pandemics. Being one of the most cri
by
Sam Coxeter
Similar jobs at ICON
Salary
Location
Regional Great Britain (Northern Ireland)
Location
Belfast
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Data Management
Job Type
Permanent
Description
The RoleAs a Risk‑Based Study Management Lead, you will provide end‑to‑end risk oversight for assigned clinical studies, ensuring risks to patient safety, data quality, and trial integrity are proacti
Reference
JR153696
Expiry date
01/01/0001
Author
Roxanne BicknellAuthor
Roxanne BicknellSalary
Location
India, Chennai
Location
Bangalore
Chennai
Trivandrum
Bengaluru
Remote Working
Remote or Office
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Data Management
Job Type
Permanent
Description
As a CDC II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.What You Will Do:Your role
Reference
JR154819
Expiry date
01/01/0001
Author
Kalpana KulasekaranAuthor
Kalpana KulasekaranSalary
Location
Taiwan, Taipei
Location
Taipei
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Data Management
Data Science
Job Type
Permanent
Description
As a Clinical Data Science Lead at ICON, you will drive data science initiatives within clinical trials, ensuring that our analyses provide meaningful insights that inform strategic decisions.What You
Reference
JR153160
Expiry date
01/01/0001
Author
Huixin "Stella" SongAuthor
Huixin "Stella" SongSalary
Location
India, Chennai
Location
Bangalore
Chennai
Trivandrum
Bengaluru
Remote Working
Remote or Office
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Systems
Job Type
Permanent
Description
As a Senior Clinical System Designer at ICON, you will design and implement advanced clinical systems that enhance trial design and execution.What You Will Do:Your experience will be key in delivering
Reference
JR151587
Expiry date
01/01/0001
Author
Kalpana KulasekaranAuthor
Kalpana KulasekaranSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Data Management
Data Science
Job Type
Permanent
Description
We have an incredible opportunity for a Senior Clinical Data Science Lead to join ICON's Full-Service IOD Clinical Data Science team. The Senior Clinical Data Science Lead (Senior CDSL) serves as the
Reference
JR151329
Expiry date
01/01/0001
Author
Tallulah PierreAuthor
Tallulah PierreSalary
Location
India, Trivandrum
Location
Bangalore
Chennai
Trivandrum
Bengaluru
Remote Working
Remote or Office
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Data Management
Job Type
Permanent
Description
As a CDC II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do:Your rol
Reference
JR153699
Expiry date
01/01/0001
Author
Kalpana KulasekaranAuthor
Kalpana Kulasekaran