LocationBuenos Aires, Argentina (Complejo LUMINA – Office Park).
Hybrid model: 2–3 days per week in office.How to ApplyPlease submit your resume in English when applying.OverviewUse Your Power for Purpose.
Our mission is straightforward: support healthcare decisions that ensure the safe and effective use of medications.
Whether you are developing the framework to ensure our evidence is scientifically robust, providing unbiased and medically essential expertise, or exploring ways to bridge data gaps, your role is vital.
By ensuring our evidence is sound and offering necessary medical insights, we strive to improve patient care and treatment efficacy.ResponsibilitiesServe as Lead Data Manager for one or more clinical trials, responsible for CDS activities including selection and application of data acquisition standards, database design, Data Management Plan, data review and query management, data access and visualization, metrics reporting, database release, and submission related activities.Independently lead daily DM activities and allocate study DM resources.Coach junior Data Managers and perform peer review of study DM deliverables.Ensure milestones met on time with good quality.Collaborate with Clinical Data Scientist to ensure operational excellence across all CDS deliverables.Adhere to SOPs and ensure study‐specific CDS documents in the Trial Master File are high quality and filed promptly.Document lessons learned and share with other study teams.Contribute to DM continuous improvement activities.QualificationsMinimum 3 years of Data Management experience.Bachelor's degree (minimum).
Demonstrated knowledge of clinical development process (GCP, FDA, ICH, GCDMP).
Proficient experience using commercial clinical data management systems and/or EDC products (e.g., Inform).
Experience using data visualization tools (e.g., Spotfire, J‐Review) is preferred.Familiarity with MedDRA/WHO‐Drug.Proficiency in Microsoft Office Suite (Outlook, Word, Excel).
Strong verbal and written communication skills, including remote communication.Project‐management skills in resource management, timeline, and quality control (preferred).
Preferred QualitiesMaster's degree.Relevant pharmaceutical industry experience.Experience using commercial clinical data management systems and/or EDC products.Awareness of regulatory requirements and relevant data standards.Strong analytical and problem‐solving skills.Ability to work collaboratively in a team environment.Excellent organizational and time‐management skills.Experience using AI tools, including generative technologies such as ChatGPT or Microsoft Copilot.Curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices.EEO StatementPfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.
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📌 Senior Associate, Senior Data Manager, Clinical Data Sciences (San Isidro)
🏢 Pfizer
📍 San Isidro