Clinical Research Associate
This role involves monitoring clinical trials and ensuring protocol compliance and data integrity. ICON offers career development, a collaborative environment, and various well-being benefits.
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88,000+ live jobsPermanent contract
Per the ad.
Fully remote
Per the ad.
Have the right to work in Spain
ICON plc doesn't mention sponsorship in the ad.
Work in English
English is required, per the ad.
University degree
“Degree in Statistics, Biostatistics, Epidemiology, Health Economics, Mathematics, Public Health or a related quantitative discipline.” — per the ad.
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:
The role is ideally suited to someone with strong SAS programming skills, proficiency in R, and a passion for applying statistical methods to healthcare and research data.
You will bring strong statistical programming skills together with an interest in Real World Evidence and healthcare research.
Required Qualifications and Experience
Degree in Statistics, Biostatistics, Epidemiology, Health Economics, Mathematics, Public Health or a related quantitative discipline.
Experience working with statistical analyses and healthcare or research data.
Strong SAS programming skills, including:
Data step programming
Conditional statements and variable creation
Data merges and concatenation
Output Delivery System (ODS)
Statistical procedures
Experience using advanced SAS techniques such as repeated measures analysis, survival analysis, SAS/Graph or advanced macros.
Proficiency in R programming.
Ability to develop statistical outputs, tables and graphs.
Strong analytical, organisational and problem-solving skills.
Effective written and verbal communication skills.
Ability to work collaboratively within a team environment.
Strong SAS programming skills and proficiency in R are essential requirements for this role and will be key areas of focus throughout the selection process.
Preferred Experience
Experience within a Real World Evidence environment.
Knowledge of epidemiology, health economics, patient-reported outcomes or related disciplines.
Experience participating in conference presentations, publications or scientific communications.
Experience supporting proposal or business development activities.
JR156832 Statistical Scientist
We are currently seeking a Statistical Scientist to join our Biostatistics & Medical Writing (BMW) Real World Evidence team.
This is an exciting opportunity to work on a diverse range of Real World Evidence projects, supporting study design, statistical analysis, programming, reporting and scientific communication activities. You will work closely with colleagues across Biostatistics & Medical Writing, contributing to the delivery of high-quality statistical outputs for clients while supporting proposal activities, publications and departmental initiatives.
Contribute to project conception and study design activities.
Support proposal development for both full-service and statistics-only projects.
Perform statistical analyses using SAS and R.
Develop and maintain SAS programs for data manipulation, analysis and reporting.
Create variables, perform data merges and prepare analytical datasets.
Apply appropriate statistical procedures to support project objectives.
Use advanced SAS techniques such as repeated measures, survival analysis, SAS/Graph, advanced macros or similar methodologies.
Develop outputs including tables, graphs and project deliverables.
Support scientific communication activities including conference presentations and publications.
Participate in professional activities and technical conferences.
Attend weekly BMW meetings and contribute to departmental initiatives.
Support Directors and members of the Executive Team with BMW initiatives.
Contribute to budgeting and scope development activities with appropriate oversight.
Adhere to departmental SOPs and quality standards.
Undertake other reasonably related duties as required.
Travel domestically and internationally as needed (approximately 5%).
Demonstrate and uphold ICON's commitment to People, Clients and Performance.
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As part of the Real World Evidence team, you will have the opportunity to contribute to a broad range of research projects while working alongside experienced statistical and scientific professionals. You'll be involved in meaningful work that supports evidence generation, healthcare decision-making and client success, while continuing to develop your technical and scientific expertise.
Visit our careers site to
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.
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