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

Why Patients Need You

As part of the Clinical Data Science (CDS) group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, Database Analysts are responsible for the programming of high-quality clinical databases. 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.
 

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.

How You Will Achieve It

• Contribute to completion of project milestones and organize own work to meet project task deadlines.

• Participate in Data Monitoring and Management (DMM) activities including data review and query management.

• Ensure quality database design including documentation, testing, validation, and implementation of clinical data collection tools, and/or other data collection systems.

• Ensure work is carried out in accordance with applicable Standard Operating Procedures (SOPs) and working practices.

• Investigate logic check flags, utilizing system information, as well as applicable study documentation.

• Liaise with Study Team Point of Contact, Document Owners, Trial master file (TMF) Study Owners and/or other end users to resolve document related discrepancies and issues.

• Identify and investigate any potential discrepancies and review findings with the study team Point of Contact to verify.

• Contribute to process improvement and additional project that may arise.

• 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.

Qualifications

Must-Have

• Bachelors degree with 1-2 years of experience.

• Demonstrated experience or knowledge of ICH/GCP (International Council for Harmonization/ Good Clinical Practice) documentation requirements.

• Hands-on experience with electronic documentation management systems and/or web based data management systems.

• Awareness of clinical development process including knowledge and understanding of the principles of Good Clinical Practice.

• Understanding of regulatory requirements and relevant data standards.

• Consistent, detail-oriented, and dedicated to excellence.

• Strong oral and written English communications skills.

• Proficiency in the use of Microsoft Office Suite of tools.

Nice-to-Have

• Experience in management of medical and clinical study records and documentation.

Other Job Details:

•  Last day to apply: November 18th, 2024

• Work Location Assignment: Position is considered Flexible, and colleagues are expected to comply with Log In For Your Day (LIFYD) requirements at site location (e.g. about 2 to 3 days a week in office).

• Eligible for Relocation Package - NO

The annual base salary for this position ranges from $64,600.00 to $107,600.00. 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