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Über diese CDC I Stelle bei ICON plc

ICON plc · Vor Ort · Mexico, Mexico City
CDC I

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 CDC I at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.


What You Will Do:

You will take responsibility for clinical research deliverables, applying your skills to ensure quality and efficiency.

What you will be doing:

  • Performs routine reviews of clinical and third-party data for subjects enrolled in clinical research protocols based on edit check/output specification documentation
  • Maintains clinical data management related study documentation as appropriate
  • May be responsible for local lab data entry and local lab data review activities as required
  • Executes data review and analytic requirements on low to medium complexity work
  • Manages third-party data reconciliation process
  • Assist Clinical Data Science Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures

Your profile:

  • 1-2 years of clinical data management experience in a clinical research organization or pharmaceutical company
  • Basic knowledge of the drug development process
  • 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-DT2


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

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Über ICON plc

ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

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