EG-Senior Associate, Data Acquisition Analyst, Clinical Data Acquisition, SH/BJ

ROLE SUMMARY

As part of the Data Monitoring and Management (DMM) group, an integral delivery unit within the Global Biometrics and Data Management organization, the Associate, Data Acquisition Assistant is responsible for the provision of operational assistant in data monitoring and management with an emphasis on Third Party Vendor data, PK/PD, Medical Lab Normal Ranges, supporting assigned studies within the Pfizer portfolio. Accountabilities to include define data file specifications, setup data loading, ensuring the integrity of clinical data, application of standards, supporting consistency in asset/submission data. The Associate, Data Acquisition Assistant works closely with Associate Director, Group Lead; Manager, Data Acquisition Lead, other Data Acquisition Analysts, Clinical Data Scientists, Clinical Data Trial Leads and Data Managers to ensure Third Party Vendor Data appropriate loaded to Pfizer clinical databases supporting the Pfizer portfolio with consistent, timely and high quality application of technology, data standards and processes. 

ROLE RESPONSIBILITIES

• Provide technical solution in assigned functional areas, including but not limited to: Vendor Qualification Assessment, Data transfer specifications creation, Test Data Review, Data review model creation and Data loading monitoring, LNMT Setup under supervision
• Ensure vendor consistent use Data Transfer Specifications per data standards. The ultimate objective is to ensure data quality and consistency across programs and repositories.
• Collaborate with other Data Acquisition Analysts to develop and maintain a support model and to facilitate issue resolution and capture corrective actions; and to ensure operational efficiencies such as sharing of best practices across work areas, functions and sites.
• Monitor vendor data loading to align with data flow activities and create data input model for DM to perform reconciliation 
• Resolve and report any data loading quality issues to ensure data quality
• Able to resolve conflicts, influence and communicate with key stakeholders and customers.
• Technical capabilities as well as effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization.

BASIC QUALIFICATIONS

• Bachelor’s degree or above of equivalent experience in a scientific discipline required.
• Working knowledge of clinical development process, understanding concepts of Phase I-IV and principles of study design
• Knowledge of clinical trial database and its applications
• Knowledge of Windows Environment and its applications (Word, Excel, PowerPoint, Project, etc.)

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical