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Work ScheduleStandard (Mon-Fri)

Environmental ConditionsOfficeJob Description

Join Us as a Senior Clinical Data Associate – Make an Impact at the Forefront of Innovation

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance.As a

Senior Clinical Data Associate , you will perform all aspects of the data cleaning process with minimal supervision in accordance with:Good Clinical Practices (GCP)Standard Operating Procedures / Work Process Documents (SOPs/WPDs)Your work will support the assessment of the safety and efficacy of investigational products and/or medical devices.Clinical Data Management Activities

Support the setup of study activities such as:

Database designTesting of data entry screensData Validation Manual (DVM) creation as required

Review data listings for accuracy and consistencyGenerate, track, and resolve data clarifications and queriesMake changes to the clinical database as requiredSubject Matter Expertise & Process Improvement

Act as point person and subject matter expert for specialized study-specific processesContribute to the improvement of data management processes on a global levelUnderstand project protocol and DVM requirementsReporting & Collaboration





Produce project-specific status reports for management and/or clients on a regular basisProvide training and work direction to junior staff as requiredCollaborate with project teams while maintaining high quality standardsRequired:

Bachelor’s degree or equivalent and relevant formal academic/vocational qualificationExperience:

Previous experience that provides the knowledge, skills, and abilities to perform the job comparable to 0 to 2 yearsIn some cases, an equivalency consisting of a combination of appropriate education, training, and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.✅ Ability to apply knowledge and skills in a highly organized fashion while adhering to:Regulatory guidelinesGlobal SOPsClient expectations✅ Strong attention to detail and numerical skills✅ Good written and verbal communication skills✅ Good analytical and problem-solving skills✅ Ability to maintain a high degree of confidentiality with clinical and proprietary client data✅ Strong customer focus and excellent interpersonal skills✅ Proven flexibility and adaptability✅ Ability to set and meet timelines or negotiate schedule changes in response to project demands✅ Knowledge of medical/clinical terminology✅ Proven ability in achieving applicable technical competencies per the DM competency gridWork is performed in an office environment with exposure to electrical office equipmentOccasional drives to site locationsOccasional travel both domestic and internationalWhen you join Thermo Fisher Scientific, you become part of a global team that values:PassionInnovationCommitment to scientific excellenceYou’ll work in an environment where collaboration and development are part of the everyday experience — and where your contributions truly make a difference.✨

Apply today to help us deliver tomorrow’s breakthroughs.

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📌 Sr Clin Data Assoc (Ciudad de México)
🏢 Thermo Fisher Scientific
📍 Ciudad de México