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Full-time
bachelor degree
Competitive base salary, Performance related incentives, Medical coverage, Dental coverage, Vision coverage, Retirement plans
Posted 14d ago
~40 hrs/week
Remote in Ciudad de México, Mexico
Responsibilities
The Clinical Data Risk Analyst identifies and mitigates risks associated with clinical trial data to ensure integrity and regulatory compliance. They collaborate with cross-functional teams to develop risk management plans and monitor data quality throughout the trial process.
Requirements
Candidates must hold a degree in life sciences or a related field and possess at least 3 years of experience in clinical trials. Strong analytical, technical, and communication skills are required to effectively manage data risks and collaborate within global teams.
Full job description
Clinical Data Risk Analyst - Mexico - Remote
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 a Clinical Data Risk Analyst at ICON, you will identify and mitigating risks associated with clinical trial data. You will contribute to the overall success of our clinical programs by employing risk assessment methodologies to ensure data integrity and compliance with regulatory standards.
What You Will Do:
Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
Conducting risk assessments on clinical trial data to identify potential issues and recommend mitigation strategies.
Collaborating with global 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.
Your Profile:
You will bring relevant clinical research experience, along with the following qualifications and skills.
Required qualifications and experience:
Degree in life sciences or a related field.
3+ years clinical trials experience
Strong analytical and technical skills
Attention to detail and a proactive approach to identifying and addressing data risks.
Effective communication skills, with the ability to collaborate across diverse global teams and convey complex information clearly.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.
We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
Offices: ICON plc, South County Business Park, Leopardstown, Dublin, D18 X5R3, IE · 123 Smith Street, Farmingdale, New York NY 11735, US · Block 2, Hamilton House, National Technology Park, Limerick, V94 TRW8, IE · 100 Longwater Avenue, Green Park, 3rd Floor, North and South Wings, Reading, England RG2 6GP, GB · 1 Almondview Office Park, West Lothian, Livingston, EH54 6SF, GB
Medical DeviceTherapeuticsGovernment and Public Health SolutionsClinical Research ServicesCommercialisation and OutcomesOncologyValue Based HealthcareClinical TrialsPatient RecruitmentInnovation
How many Science & Research jobs are open in Ciudad de México, Mexico right now?
There are currently 339 open science & research positions in Ciudad de México, Mexico listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Ciudad de México, Mexico?
Companies currently hiring include ICON plc, Thermo Fisher Scientific, ALS, IQVIA, Boehringer Ingelheim, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in Ciudad de México, Mexico?
Yes — 193 of the 339 open science & research positions offer remote or hybrid work (90 remote, 103 hybrid).
How do I apply for Science & Research jobs in Ciudad de México, Mexico?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.