Senior Associate, Senior Data Manager, Clinical Data Sciences

Pfizer; San Isidro; Hybrid; ARS 90,873,000 - 136,310,000; Full time

Job summary

Pfizer in Buenos Aires, Argentina, is seeking a Lead Data Manager to oversee CDS activities across one or more clinical trials. You will design and test data collection tools, develop data management plans, review data quality, manage queries, and provide data access and visualization capabilities.

The role requires collaboration with study teams and ensuring TMF readiness. Minimum 3 years in data management, knowledge of GCP/FDA/ICH, and experience with EDC systems (Inform preferred) are

Qualifications

• Understand clinical development process and GCP principles.
• Experience with data management in clinical trials and regulatory standards.
• Ability to interpret protocols and determine study requirements.
• Strong communication, including remote collaboration.
• Bachelor’s degree required; Master’s preferred.
• Experience with FDA/ICH/GCP regulations and data standards.

Responsibilities

• Lead daily data management activities for one or more trials.
• Manage data acquisition standards, database design, and tooling.
• Develop and maintain the Data Management Plan and TMF documents.
• Perform data review, query management, and data visualization.
• Coordinate milestones and ensure on-time delivery with quality.
• Mentor junior data managers and perform peer reviews.
• Collaborate with Clinical Data Scientist for CDS deliverables.
• Ensure SOP compliance and cross-study knowledge sharing.
• Drive continuous improvement in DM processes.

Skills

GCP knowledge

Data management

Clinical trials knowledge

Verbal and written communication

3+ years data management experience

Regulatory knowledge (FDA, ICH, GCP)

MS Office suite

Resource management

Team coaching/mentoring

Analytical problem solving

Education

Bachelor’s degree

Master’s degree

Tools

Inform

Spotfire

J-Review

TMF/eTMF documentation

Job description

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.

Use 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.

What You Will Achieve

In this role, you will:

• 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, includingrisk 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.

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