Job Description
Introducing Global Clinical Data Integration (GCDI) Transforming clinical data management in Latin America. With a focus on streamlining information, our department collects, cleans, transforms, and archives clinical data, ensuring high quality and compliance. As a new addition to the region, we intend to enhance efficiency and leverage local information across departments to drive innovation and deliver value across clinical trials, data management standards, and technology platforms.
Our Clinical teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards.
Requirements
- Bachelor's degree, preferably in IT, computer science, mathematics, science, a healthcare-related discipline, or relevant skills and experience;
- Effective communication skills (oral and written) with the ability to communicate with both the technical and business areas in Spanish and English;
- Database design and development knowledge;
- An overall working knowledge of the clinical development process
- Knowledge of database structures and available tools to manage, extract, and report data
- Able to work under pressure and adapt to changing environments with flexibility
- Exceptional organizational and problem-solving skills;
- Ability to work cross functionally and as part of a team;
- Capable of thriving in an autonomous work settings, adapting with ease to challenging circumstances, and displaying flexibility in dynamic environments.
- An overall knowledge of database structures and available tools to manage, extract, and report data is preferred (such as Python, Java, C#, Jira, Power BI, Github, SQL);
- System Development Lifecycle Management / system validation knowledge is preferred
Responsabilities
- Perform execution of standard and trial-specific test scripts and record test data and test results
- Creation and execution of standard and trial-specific test scripts
- Develop knowledge in programming, system analysis, and testing
- Ensure all testing documentation is stored in the electronic trial master file
- Support the testing of tools and applications, including creating test plans, test scripts, and execution of test scripts
DataIntegrationLatam
DataIntegrationCOL
Required Skills
Ability to Work Under Pressure, Adaptability, Analytical Problem Solving, Clinical Data Cleaning, Clinical Testing, Data Analysis, Data Documentation, Data Review, Good Clinical Practice (GCP), Teamwork
Preferred Skills
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Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status
Project Temps (Fixed Term)
Relocation
VISA Sponsorship
Travel Requirements
Flexible Work Arrangements
Hybrid
Shift
Valid Driving License
Hazardous Material(s)
Job Posting End Date
10/14/2025
- A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID R368376
