Senior Clinical Data Risk Analyst

ICON; Ciudad de México; A distancia; USD 40,000 - 70,000; Jornada completa

Descripción de la vacante

A leading healthcare organization seeks a Senior Clinical Data Risk Analyst to join their Clinical Risk Management team. This role involves analyzing clinical trial data to identify risks and ensure data integrity. Ideal candidates will have a strong background in data analysis, excellent communication skills, and a proactive approach to risk management.

Servicios

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Employee Assistance Programme

Flexible optional benefits

Formación

• 3+ years of experience in clinical data analysis or risk management in a clinical research organization.
• Knowledge of at least 1 Clinical Data Management System.
• Ability to manage multiple studies and changing priorities.

Responsabilidades

• Conduct risk assessments on clinical trial data to identify potential issues.
• Collaborate with teams to develop risk management plans.
• Monitor data quality and integrity throughout trial process.

Conocimientos

Analytical skills

Statistical analysis

Attention to detail

Proactive problem solving

Communication skills

Educación

Bachelor’s degree in life sciences or related field

Herramientas

Statistical software

Clinical Data Management System

Descripción del empleo

Senior Clinical Data Risk Analyst - Homebased or hybrid - Mexico City

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

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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