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Centralized Data Management Sr Specialist


Warsaw, IN
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Job Details

A role at Pfizer is unlike any other. Offering talented individuals the opportunity to own a career with real impact, our people go to work each day in the knowledge that every development signifies real, positive progress. We all believe in our ability to improve the future of healthcare, and in our potential to transform millions of lives. Because in every part of the world, the work we do is reaching everyone, everywhere for almost every medical need. With this breadth of ambition comes vast opportunity, providing an environment where determined, resilient professionals can learn and grow. It creates a dynamic ownership culture of diverse personalities, where everybody has equal chance to make an important contribution to our success. Pfizer, a global leader in the biopharmaceutical industry is continuously seeking fresh new talent to join our brilliant community and share our vision for the development of innovative therapies that make the world a healthier place.

**Centralized Data Management Senior Specialist (Regulatory)**

**(location: Warsaw)**

This role will work within a team whose main focus will be to interpret the regulatory data received across different geographies, functions, divisions and ensuring key activities and regulatory systems updates are completed whilst adhering to all policies, practices and procedures.

**This is what you can look forward to:**

+ Review and interpret the data 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

+ Support global/local team members with data management workload when necessary to provide flexible support for the portfolio

+ Act as Regulatory Data SME in regions supported

+ Can support Manager and CDM leadership in the design or modification standard methods and techniques.

+ May teach or mentor other more junior staff and review work completed by other colleagues when acting in mentor role.

+ Produce country/regional reports as required

**What you offer:**

+ Academic Degree: Professional in Pharmaceutical Chemistry or equivalent

+ Regulatory knowledge and experience (at least 4-5 years)

+ Demonstrated ability to work in a highly regulated environment

+ Project Management Experience

+ Proven technical aptitude and ability to quickly learn and use new software, regulations and quality standards

+ Ability to work with accuracy and attention to detail

+ Ability to work with autonomy and/or part of a team in a busy environment

+ Experience in multitasking, international environment

+ Computer literacy in MS Word/Outlook/Excel/Adobe Acrobat

+ Very good level of spoken and written English - additional language will be a strong asset

**What we offer:**

+ Employment contract and necessary tools

+ Annual bonus eligibility

+ Medical care, life-insurance, Multisport etc.

+ International environment and great development opportunities

**Please apply with English Documents only!**

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