Pfizer careers Hiring Centralized Data Management - Data Associate Professional in Pharmaceutical Chemistry Apply Now
Primary Responsibilities
Review and interpret the data provided by the PCO to
establish the system / tools required to be populated in line with current
standard operating procedures or business process documentation, including
systems and SOPs associated with the regulatory data scope.
Perform data entry and quality control tasks associated in
all global regulatory systems impacted, including systems associated with the
regulatory data scope.
Review audit reports from the systems and resolve errors to
ensure integrity of data
Identifies issues and provides input into solutions
Accountable for remediation efforts associated with their
scope as part of SCC global rollout.
Perform monthly PEARL compliance report review and complete
remediation activities in close partnership with Regulatory strategist teams
Adhering to quality control procedures and standards related
to the systems or tools ensuring Regulatory Compliance
Support global/local team members with data management
workload when necessary to provide flexible support for the portfolio.
Adhere to Pfizer compliance standards
Act as Regulatory Data SME in regions supported
Produce country/regional reports as required
Support audit as part of regulatory data / system scope
Technical Skill Requirements
Computer literacy in MS Word/Outlook/Excel/Adobe Acrobat.
Proven technical aptitude and ability to quickly learn and
use new software, regulations and quality standards
Functional and technical knowledge and skills to do the job
at a high level of accomplishment
Proven technical aptitude
Quick learner with ability to multi-task
Ability to work with accuracy and attention to detail
Ability to work with autonomy and/or part of a team in a busy
environment
Demonstrated ability to work in a highly regulated
environment
Quality focus
Customer orientation
Analysis and solution of problems
Effective communication
English intermediate to advance (written and spoken)
Qualifications (i.e., preferred education, experience,
attributes)
Academic Degree: Professional in Pharmaceutical Chemistry
Regulatory knowledge and experience (at least 1-2 years)
Demonstrated ability to work in a highly regulated
environment
Project Management Experience desirable
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