Associate, Database Analyst Clinical Database Management

Key Skills

Python Programming, SQL, Cloud computing

Job Description

Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.

What You Will Achieve

It is our mission to strengthen the oversight of our clinical data through stronger ownership, control, and visibility. You will play an important role in processing, reviewing and receiving clinical data and records and from therapeutic groups as well as internal and outside investigators. You will ensure that accurate, timely, and consistent data reaches the clinical teams and other groups. You will be relied on for data management plans including data preparation and validation activities, among others.

As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative team environment for your colleagues.

It is your commitment and hard work that will help make Pfizer ready to achieve new milestones and help patients across the globe.

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