Database (programming) Analyst (Associate), Clinical Data Management

Employer
Pfizer
Location
Groton, Connecticut
Salary
Competitive
Posted
Sep 13, 2021
Closes
Sep 26, 2021
Ref
563848
Jobseeker Type
Professional
Organization Type
Corporate
Hours
Full Time
ROLE SUMMARY:

As part of the Data Monitoring and Management (DMM) group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the 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.

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 QUALIFICAITONS
  • 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 preferred.


  • This role can be located at any of the listed locations.
  • Eligible for Employee Referral Bonus: YES


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EEO & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.

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