Senior Clinical Data Risk Analyst

ICON Clinical Research; Ciudad de México; A distancia; MXN 1,007,000 - 1,375,000; Jornada completa

Descripción de la vacante

A leading clinical research organization is looking for a Senior Clinical Data Risk Analyst to lead risk management in clinical studies. This role requires over 3 years of experience in clinical data analysis and risk management, strong analytical skills, and familiarity with various clinical data management systems. Ideal candidates will effectively collaborate and communicate across teams. The position is based in Mexico or Colombia and offers competitive salary and benefits.

Servicios

Health insurance

Retirement planning

Flexible optional benefits

Formación

• 3+ years of experience in clinical data analysis or risk management.
• Strong proficiency in statistical software.
• Attention to detail with proactive data risk identification.

Responsabilidades

• Conduct risk assessments on clinical trial data.
• Collaborate to develop risk management plans.
• Monitor data quality throughout the trial process.

Conocimientos

Clinical data analysis

Risk management

Analytical skills

Communication skills

Educación

Bachelor’s degree or equivalent in life sciences

Herramientas

Medidata RAVE

InForm

Veeva

Descripción del empleo

Overview

Senior Clinical Data Risk Analyst - Homebased - Mexico or Colombia

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 Clinical Data Risk Analyst to join ICON’s Full Service IOD Clinical Risk Management team. The CDRA is a clinical risk management and central monitoring functional lead. The CDRA is responsible for clinical data analysis components of clinical studies, including RBQM facilitation, planning, selection of KRIs focusing on identified risks, advanced analytics design and programming specifications, review of centrally aggregated data to identify risk and issues impacting data integrity, patient safety, and regulatory compliance.

What you will be doing

• Conducting risk assessments on clinical trial data to identify potential issues and recommend mitigation strategies
• Collaborating with cross-functional teams to develop and implement risk management plans and protocols
• Monitoring data quality and integrity throughout the trial process, reporting findings to stakeholders
• Utilizing statistical analysis and visualization tools to communicate risk-related insights effectively
• Supporting the preparation of risk management documentation for regulatory submissions and audits
• Providing mentoring for junior staff

Your profile

• 3+ years of experience in clinical data analysis or risk management in a clinical research organization or pharmaceutical company
• Strong analytical skills with proficiency in statistical software and risk assessment methodologies
• Attention to detail and a proactive approach to identifying and addressing data risks
• Knowledge of at least 1 Clinical Data Management System (Medidata RAVE, InForm, Veeva, Cluepoints, Medidata Detect, JReview, etc.)
• Ability to manage multiple studies simultaneously while handling changing priorities and competing deadlines
• Excellent written and oral communication skills
• Bachelor’s degree or local equivalent (in life sciences or related field preferred)
• 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

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 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 apply through the internal link.