
Breakthroughs that change patients' lives.
Associate, Associate Database Analyst
ROLE SUMMARY
As part of the Clinical Data Sciences (CDS) group, an integral delivery unit within the Clinical Development & Operations (CD&O) organization, the Associate Database Analyst is responsible for the programming of high-quality clinical databases. Responsible for supporting assigned segments of the Pfizer portfolio. Accountabilities to include the design, development, and maintenance of clinical databases, ensuring the integrity of clinical data, application of standards supporting consistency in asset/submission data. The Associate Database Analyst works with senior staff members to understand Pfizer standard database conventions and begins to understand the nuances of data collection needs between therapy areas
ROLE RESPONSIBILITIES
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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
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Complies with applicable SOPs and work practices
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Develops expertise in one or more technologies
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Develops knowledge of data capture tools and methods that support the accuracy and integrity of study data
BASIC QUALIFICATIONS
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Bachelor's degree in a Life Science, Computer Science or equivalent
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Minimum 2 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions
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Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills
PREFERRED QUALIFICATIONS
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Technical skills and experience using relational databases (e.g. Oracle In Form, Oracle DMW, MS SQL Server or MS Access)
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Strong communication (written and oral), decision-making, influencing, negotiation, and project management skills
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Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)
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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.)
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Understanding of regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable
Work Location Assignment: Hybrid
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
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About Pfizer

Pfizer
PublicPfizer Inc. is an American multinational pharmaceutical and biotechnology corporation headquartered at The Spiral in Manhattan, New York City. Founded in 1849 in New York by German entrepreneurs Charles Pfizer (1824–1906) and Charles F.
10,001+
Employees
New York City
Headquarters
$280B
Valuation
Reviews
10 reviews
4.0
10 reviews
Work-life balance
3.2
Compensation
4.3
Culture
4.1
Career
3.4
Management
3.5
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Pros
Good salary and competitive compensation
Supportive management and team collaboration
Innovative and interesting projects
Cons
High workload and overwhelming demands
Long hours and fast-paced environment
Limited career advancement opportunities
Salary Ranges
11 data points
Junior/L3
Mid/L4
Senior/L5
L3
Junior/L3 · SENIOR ASSOCIATE SCIENTIST
1 reports
$86,450
total per year
Base
$66,500
Stock
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Bonus
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$86,450
$86,450
Interview experience
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Difficulty
3.0
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Duration
14-28 weeks
Interview process
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Application Review
2
HR Screen
3
HireVue Video Interview
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Hiring Manager Interview
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Final Interview/Panel
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Offer Decision
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Behavioral/STAR
Past Experience
Culture Fit
Technical Knowledge
Case Study
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