Senior Associate, Senior Data Manager, Clinical Data Sciences

Pfizer, S.A. de C.V; Buenos Aires; Vor Ort; ARS 600.000 - 900.000; Vollzeit

Benefits dieser Stelle

Competitive compensation

Diverse benefits programs

Zusammenfassung

Pfizer, S.A. de C.V is seeking a Senior Associate, Senior Data Manager in Buenos Aires, Argentina. In this role, you will lead Data Management activities for clinical trials and ensure operational excellence while collaborating with cross-functional teams. The position requires strong Data Management experience and a Bachelor's degree.

This hybrid role requires you to work from the Pfizer office 2–3 days per week. Join us to contribute to breakthroughs that change patients’ lives and be part of an innovative team focused on improving healthcare.

Qualifikationen

• Minimum 3 years of Data Management experience required.
• Demonstrated knowledge of clinical development process.
• Proficient experience using commercial clinical data management systems.

Aufgaben

• Serve as Lead Data Manager for clinical trials.
• Independently lead daily DM activities.
• Coach junior Data Managers in the study.

Kenntnisse

Data Management

Clinical Development

Communication skills

Project Management

Ausbildung

Bachelor’s degree

Tools

Clinical data management systems

Data visualization tools

Microsoft Office Suite

Jobbeschreibung

Senior Associate, Senior Data Manager, Clinical Data Sciences

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life‑changing medicines to the world.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

Application Instructions

Please submit your resume in English when applying.

Work Location Assignment

Buenos Aires, Argentina (Complejo LUMINA – Office Park). This role follows a hybrid model. Colleagues are expected to work from the assigned Pfizer office 2–3 days per week, or as required by business needs.

What You Will Achieve

• Serve as Lead Data Manager for one or more clinical trials assuming responsibility for CDS activities including selection and application of data acquisition standards, database design (including specification documentation and testing of clinical data collection tools, both CRF and non‑CRF, using an EDC system and/or other data collection systems), development and maintenance of the Data Management Plan, data review and query management, data access and visualization, Data Management metrics reporting, database release, and submission related activities.
• Independently lead the daily DM activities and allocate study DM resource in the appropriate way.
• Coach junior Data Managers in the study and perform peer review of study DM's deliverables for quality control.
• Be responsible to achieve the study DM milestone on time with good quality.
• In collaboration with the Clinical Data Scientist, ensure operational excellence across all CDS deliverables.
• Ensure work carried out in accordance with applicable SOPs and working practices.
• Ensure the required study‑specific CDS documents in the Trial Master File (TMF) are of high quality and are filed contemporaneously to support downstream inspection and submission readiness activities.
• Ensure operational excellence in collaboration with CDS for application of standards, data acquisition, proactive data review and query management, data cleaning, e‑data processing, data access and visualization, DM metrics reporting, database release, and submission related activities.
• Ensure lessons learnt during the course of the study are documented and shared with other study teams to facilitate cross‑study learning.
• Be capable to contribute on the DM related continuous improvement activities.

Here Is What You Need (Minimum Requirements)

• Demonstrated knowledge of clinical development process including knowledge and understanding of the principles of GCP.
• Demonstrated knowledge of data management processes and principles in area of responsibility.
• Working knowledge of all phases of clinical trials and ability to assess and determine study requirement from protocol review.
• Demonstrates strong verbal and written communication skills including ability to communicate remotely.
• Minimum 3 years Data Management experience required.
• Working knowledge of clinical research, FDA & ICH, GCP, GCDMP, and related regulatory requirements.
• Proficient experience using commercial clinical data management systems and/or EDC products (e.g. Inform preferred).
• Experience using data visualization tools (e.g. Spotfire, J‑Review) preferred.
• Familiarity with MedDRA/WHO‑Drug.
• Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.).
• Bachelor’s degree minimum requirement.
• Experience of project management skill in terms of resource management and timeline and quality control preferred.

Bonus Points If You Have (Preferred Requirements)

• Master's degree.
• Relevant pharmaceutical industry experience.
• Experience using data visualization tools.
• Proficient 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 common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use.

EEO (Equal Employment Opportunity) & Employment Eligibility

Pfizer 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.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI‑use guidelines available on Pfizer Careers.