sr. Associate, data manager, clinical data sciencesPfizer
Workplace: MetroManila, Manila, Makati
Salary: Agreement
Work form: Full time
Posting Date: 10/02/2026
Deadline: 29/06/2021
Role Summary
As part of the Data Monitoring and Management group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Data Manager is responsible for timely and high quality data review and query management of clinical data supporting the Pfizer portfolio. The Data Manager executes on key data management deliverables used to collect, review, monitor, and ensure the integrity of clinical data.
Role Responsibilities
Participate in DMM activities including data review and query management, assist with quality database design including documentation, testing, validation, and implementation of clinical data collection tools, CRF and non-CRF, using an electronic data capture (EDC) system and/or other data collection systems, supporting the database set up activities as assigned by Senior Data Manager or Clinical Data Scientist.
Ensure work carried out in accordance with applicable SOPs and working practices.
Assist with the required study-specific DMM documents in the Trial Master File (TMF) are of high quality and are filed contemporaneously to support downstream inspection and submission readiness activities.
Assist with operational excellence in collaboration with SR. Data Manager and 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.
Qualifications & Skills
Bachelor's degree minimum requirement. Health Sciences experience or Technology degree preferred.
2-5 years of experience in Clinical Data Management, performing complete data review activities, in a CRO or a Pharma Company.
Awareness of clinical development and pharmaceuticals as a regulated industry
Awareness of healthcare regulatory authorities (e.g. FDA, Health Canada)
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)
Awareness of MedDRA/WHO-Drug preferred
Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
#LI-PFE
Pfizer
As part of the Data Monitoring and Management group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Data Manager is responsible for timely and high quality data review and query management of clinical data supporting the Pfizer portfolio. The Data Manager executes on key data management deliverables used to collect, review, monitor, and ensure the integrity of clinical data.
Role Responsibilities
Participate in DMM activities including data review and query management, assist with quality database design including documentation, testing, validation, and implementation of clinical data collection tools, CRF and non-CRF, using an electronic data capture (EDC) system and/or other data collection systems, supporting the database set up activities as assigned by Senior Data Manager or Clinical Data Scientist.
Ensure work carried out in accordance with applicable SOPs and working practices.
Assist with the required study-specific DMM documents in the Trial Master File (TMF) are of high quality and are filed contemporaneously to support downstream inspection and submission readiness activities.
Assist with operational excellence in collaboration with SR. Data Manager and 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.
Qualifications & Skills
Bachelor's degree minimum requirement. Health Sciences experience or Technology degree preferred.
2-5 years of experience in Clinical Data Management, performing complete data review activities, in a CRO or a Pharma Company.
Awareness of clinical development and pharmaceuticals as a regulated industry
Awareness of healthcare regulatory authorities (e.g. FDA, Health Canada)
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)
Awareness of MedDRA/WHO-Drug preferred
Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
#LI-PFE
Pfizer
Other Info
Makati City, Metro Manila
Permanent
Full-time
Permanent
Full-time
Submit profile
Pfizer
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