Clinical Data Coordinator I
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What you'll do
- 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
What they're looking for
- 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
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
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.
We have an incredible opportunity for a Clinical Data Coordinator I to join ICON’s Full Service IOD Clinical Data Science team. The CDC I supports and executes the data review activities that contribute to delivery of clinical data that meets agreed upon data integrity standards.
Locations:
- Mexico City (office-based an average of 3 days per week)
- Colombia (home-based or hybrid)
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
Company
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