Clinical Data Associate II: Drive Data Quality and Impact

ThermoFisher Scientific; México; Remote; MXN 240,000 - 420,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Clinical Data Associate II to support data management activities within pharmaceutical trials. The role emphasizes accuracy, adherence to GCPs and SOPs, and is responsible for assessing safety and efficacy data across multiple studies.

Responsibilities include resolving data discrepancies, generating data listings, and conducting data management reviews to ensure high-quality data for regulatory submissions and client reporting.

Qualifications

• High/Secondary school diploma or equivalent and relevant formal academic / vocational qualification
• Technical positions may require a certificate
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 6 years)

Responsibilities

• Identify, resolve, and update data discrepancies. Make changes to the data management database as required.
• Generate, track and resolve data clarifications and queries. May implement CRF design in identified graphic design package.
• Review data listings for accuracy and consistency of data. Analyze and resolve data validation and other data management reports.
• Produce project-specific status reports for CDM management and for clients on a regular basis.
• Perform data management activities such as Serious Adverse Event and Third Party Vendor reconciliations as well as Data Listing reviews.

Skills

Data management

Attention to detail

Regulatory compliance

English proficiency

Communication skills

Education

High school diploma or equivalent

Job description

Thermo Fisher Scientific is seeking a Clinical Data Associate II to support data management activities within pharmaceutical trials. The role emphasizes accuracy, adherence to GCPs and SOPs, and is responsible for assessing safety and efficacy data across multiple studies.

Responsibilities include resolving data discrepancies, generating data listings, and conducting data management reviews to ensure high-quality data for regulatory submissions and client reporting.