Pfizer

pharmaceutical

AssociateDatabaseAnalyst,ClinicalDatabaseManagement

Greece FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“Associate Database Analyst, Clinical Database Management at Pfizer. Skills: Clinical Databases, Database Programming, Data Integrity. Programming high-quality clinical databases. Supporting assigned segments of Pfizer portfolio”

What You'll Achieve.

timely delivery of data; accuracy and integrity of study data

Industry & Context.

pharmaceutical
Problems you'll solve

decision-making

What They're Looking For.

Must Have

Bachelor's degree in a Life Science, Computer Science or equivalent, Minimum of 1 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions, Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills

Nice to Have

Technical skills and experience using relational databases (e. g. Oracle InForm, Oracle DMW, MS SQL Server or MS Access), communication (written and oral), decision-making, influencing, negotiation, and project management skills, Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc. ), Understanding of drug development process and data operations required for the reporting of clinical trial data (e. g. data review, study reports, regulatory submissions, safety updates, etc. ), Understanding of regulatory requirements and relevant data CDISC knowledge and experience are preferable

What You'll Do.

Programming high-quality clinical databases

Supporting assigned segments of Pfizer portfolio

and maintenance of clinical databases

Ensuring integrity of clinical data

Application of standards supporting consistency

Create data capture solutions

Support quality and timely delivery of data

Complies with applicable SOPs

Learns Pfizer database technologies

Develops knowledge of data capture tools

How You'll Work.

Team & Collaboration

Works closely with department roles; Works closely with cross-functional study team members

Communication Scope

communication (written and oral)

Process & Methodology

project management skills

Full Job Description

**ROLE SUMMARY** As part of the Clinical Data Sciences (CDS) group, an integral delivery unit within the Clinical Development & Operations (CD&O) organization, the Database Analyst is responsible for the programming of high-quality clinical databases and supporting assigned segments of the Pfizer portfolio. Accountabilities include the design, development, and maintenance of clinical databases, ensuring the integrity of clinical data, application of standards supporting consistency in asset/submission data. **ROLE RESPONSIBILITIES** * Works closely with department roles and cross-functional study team members to create data capture solutions that support the quality and timely delivery of data required per standard and study specific data review plans * Complies with applicable SOPs and work practices * Learns Pfizer database technologies * Develops knowledge of data capture tools and methods that support the accuracy and integrity of study data **BASIC QUALIFICATIONS** * Bachelor's degree in a Life Science, Computer Science or equivalent * Minimum of 1 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions * Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills **PREFERRED QUALIFICATIONS** * Technical skills and experience using relational databases (e.g. Oracle InForm, Oracle DMW, MS SQL Server or MS Access) * Strong communication (written and oral), decision-making, influencing, negotiation, and project management skills * Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.) * Understanding of drug development process and data operations required for the reporting of clinical trial data (e.g. data review, study reports, regulatory submissions, safety updates, etc.) * Understanding of regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable Wor

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