Associate Clinical Data

About the job HCLTech is a global technology company, home to more than 218,000 people across 59 countries, delivering industry-leading capabilities centered around digital, engineering, cloud and AI, powered by a broad portfolio of technology services and products. We work with clients across all major verticals, providing industry solutions for Financial Services, Manufacturing, Life Sciences and Healthcare, Technology and Services, Telecom and Media, Retail and CPG, and Public Services. Consolidated revenues as of 12 months ending September 2024 totaled $13.7 billion. ROLE RESPONSIBILITIES Perform activities, including but not limited to: the testing of CRF design, Database building, Acquisition & Processing of electronic data such as external eData, Lab Data, ECG Data, PK/PD Data, etc. Data extraction, Data Visualization; Data and Documentation Processing, CRF and Database edit checks/validation and validation of exceptional reports/listings. Accountable for high quality and on time delivery for assigned deliverables. Ensure the consistent use and application of applicable data standard and ensures data quality and consistency across programs and repositories. Solid knowledge/understanding of the Software development, Lifecycle testing methodology; document management. Participate in initial Data Management meetings with Clinical Data Scientist or Study Data Manager to understand the expectation and scope of the study requirements. Ensure work carried out in accordance with applicable standard operating procedures and working practices. Understand the Protocol and provide input to Study Team on Database Design and Edit Check Specification as appropriate. Review the Edit Check Specification, write UAT test Scripts. May perform the peer review for programming checks. May perform the QC on metadata listings. Participate in UAT feedback meetings. Streamline/Standardize the Scripts for Standard Forms/Edit Checks. Validation of Manual queries/Listings (Standards/Therapeutic Specific). Able to understand the Post Production Changes in Database during conduct and provide clinical/technical suggestion. Track the lessons learned and share the knowledge across the team. Complete all the documentation related to study and share it with study Team. BASIC QUALIFICATIONS Bachelor’s degree minimum requirement. Health Sciences experience or Technology degree preferred. Zero to 4 years’ experience in Clinical Data Management, performing complete data review activities, in a CRO or a Pharma Company. Ability to learn clinical data management processes and principles in area of responsibility. Demonstrates required verbal and written communication skills including ability to communicate remotely Capable to learn technical data systems Capable to learn how to use data visualization tools (e.g. Spotfire, J-Review) Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.) PREFERRED QUALIFICATIONS Experience writing test cases and performing UAT preferred Experience within a database management role, understanding key processes and principles associated with CRF design, database set-up, edit check specification, data transfer activities is preferred Awareness of clinical development and pharmaceuticals as a regulated industry Awareness of healthcare regulatory authorities (e.g. FDA, Health Canada) We offer a competitive package that includes Life insurance Major Medical Expenses Insurance Minor Medical Expense Insurance Savings Fund 13% Food vouchers 10% 30 days as Christmas Bonus 12 days of vacation in the first year, increasing 2 days as dictated by law. Additionally, we provide continuous training and development opportunities to help our employees achieve their professional goals. We need Fluent English

Location: Mexico City, Mexico, MX

Posted Date: 10/5/2025