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Database Analysts; Associate--Clinical Data Collection Strategies

Job in New York, New York County, New York, 10261, USA
Listing for: Pfizer, S.A. de C.V
Full Time position
Listed on 2026-09-05
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 68600 - 114300 USD Yearly USD 68600.00 114300.00 YEAR
Job Description & How to Apply Below
Position: Database Analysts (Associate)--Clinical Data Collection Strategies
Location: New York

Database Analysts (Associate)--Clinical Data Collection Strategies

  • United States
    - New York
    - Pearl River
  • United States
    - Connecticut
    - Groton
  • United States
    - Pennsylvania
    - Collegeville
  • United States
    - New York
    - New York City

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

You will be responsible forthe programming of high-quality clinical databases.

You will support assigned segments of the Pfizer portfolio.

Your responsibilities will 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

Work closely with department roles and cross-functional study team members to create data capture solutions that support the quality andtimelydelivery of datarequiredper standard and study specific data review plans

Complies with applicable SOPs and work practices

Develops knowledge of data capture tools and methods that support the accuracy and integrity of study data

MINIMUM
QUALIFICATIONS

Bachelor's degree in a Life Science discipline, Computer Science or other relevant discipline

Minimum of1year 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

Strong communication skills—written, verbal and presentation

Proficiency in the use of Microsoft Office Suite of tools (e.g., Outlook, Word, Excel)

PREFERRED QUALIFICATIONS

Experience using relational databases (e.g.,Oracle InForm, Oracle DMW, MS SQLServeror MS Access)

Understanding of drug development process and data operationsrequiredfor the reporting of clinical trial data (e.g.data review, study reports, regulatory submissions, safety updates)

Understanding of regulatory requirements and relevant data standards

Work Location: Must work on-site an average of 2.5 days per week and live within commuting distance to the site.

The annual base salary for this position ranges from $68,600.00 to $. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage.

Learn more at Pfizer Candidate Site – U.S. Benefits | (usca). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

This role is posted in multiple locations. If you are applying for the role in an secondary job posting location where pay transparency regulations apply, your Talent Advisor will share the local pay information with you during the first interview.

ROLE SUMMARY

You will be responsible forthe programming of high-quality clinical databases.

You will support assigned segments of the Pfizer portfolio.

Your responsibilities will 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

  • Work closely with department roles and cross-functional study team members to create data capture solutions that support the quality andtimelydelivery of datarequiredper standard and study specific data review plans

  • Complies with applicable SOPs and work practices

  • Le…

Position Requirements
10+ Years work experience
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