Associate Database Programmer Analyst, Clinical Database Management

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2 Locations
Hybrid
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
ROLE SUMMARY
As part of the C linical Data & Information Sciences (CDIS) g roup, an integral delivery unit within the Clinical Development & Operations (CD&O) organization, the Database Analyst is responsible for the programming of high-quality clin ic al 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 s tudy 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
  • Any years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions will be considered as a plus
  • 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 sub missions, safety updates, etc.)
  • Understanding of regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable

Please apply by sending your CV in English.
Work Location Assignment: Hybrid
Purpose
Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.
Digital Transformation Strategy
One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.
Flexibility
We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let's start the conversation!
Equal Employment Opportunity
We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms - allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.
Disability Inclusion
Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!
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