Senior CDC

ICON Clinical Research; Bogotá ciudad; Híbrido; COP 249.120.000 - 373.680.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme (

Descripción de la vacante

ICON Clinical Research is seeking a Senior Clinical Data Coordinator to support Colombia (Remote) and Mexico (Hybrid). You will lead data management tasks, ensure data quality, and collaborate with cross-functional teams across studies.

The role requires 3.5+ years in clinical data management and experience with CDMS like Medidata RAVE, InForm or Veeva, plus strong English and local language skills. You will mentor junior staff to help meet study timelines.

Formación

• 3.5+ years of clinical data management experience in a CRO or pharmaceutical company.
• English and host country language proficiency required.
• Strong knowledge of Windows and MS Office and standard software.

Responsabilidades

• Create and maintain data management plans and documentation.
• Identify and resolve data discrepancies to improve data quality across studies.
• Collaborate with clinical operations and biostatistics to implement data management strategies.
• Handle study documentation, queries, and archiving to support timelines.
• Mentor junior data coordinators on reconciliation, coding and cleaning procedures.

Conocimientos

Fluent English

Communication skills

Microsoft Office

Educación

Bachelor's degree or local equivalent

Herramientas

Medidata RAVE

InForm

Veeva

Descripción del empleo

Senior Clinical Data Coordinator (Sr CDC) - Colombia (Remote) and Mexico (Hybrid)

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

What You Will Do:

You will lead on clinical research tasks requiring technical depth, with a focus on quality and continuous improvement.

Key responsibilities include:

• Create and maintain detailed data management plans and documentation, ensuring compliance with industry standards and regulatory requirements.


• Participate in the identification and resolution of data discrepancies and issues, working to streamline data flow and enhance data quality throughout the study lifecycle.


• Collaborate closely with cross-functional teams, including clinical operations and biostatistics, to develop and execute data management strategies tailored to specific studies.


• Perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation , dispatching of queries to investigator sites for resolution, etc.).


• Mentor junior data coordinators, providing expert guidance on data reconciliation, coding, and cleaning procedures.

Your Profile:

You will have a strong foundation in clinical research, with the experience to work independently and guide others.

Required qualifications and experience:

• 3.5 + years of clinical data management experience in a clinical research organization or pharmaceutical company


• Intermediate 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.

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.

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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.

Are you a current ICON Employee?