Welcome to shopdeal.testchamberhub.com info We provide job seekers with information gathered from various publicly available job posting websites, including but not limited to Google, Indeed, LinkedIn, and other well-known job platforms. Our mission is to help individuals find employment opportunities by offering up-to-date job listings and career-related resources. We do not charge any fees for accessing or using our website, and all job information is provided free of charge.
shopdeal.testchamberhub.com. does not directly offer, manage, or engage in the hiring process for any of the job listings featured on our website. All listings are sourced from third-party job posting platforms such as Indeed, LinkedIn, and other recognized job websites.
By using our website, you acknowledge and accept the above terms and conditions. Thank you for visiting shopdeal.testchamberhub.com, and we wish you success in your job search.
As part of the Clinical Data Collection Strategies (CDCS) group, an integral delivery unit within the Clinical Development Information Sciences (CDIS) 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.
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
Requirements
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-haves
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
Benefits
401(k) plan with Pfizer Matching Contributions
additional Pfizer Retirement Savings Contribution
paid vacation
holiday and personal days
paid caregiver/parental and medical leave
health benefits to include medical, prescription drug, dental and vision coverage