Database (programming) Analyst (Associate), Clinical Data ManagementUnited States - Massachusetts - CambridgeUnited States - New York - Pearl RiverUnited States - Pennsylvania - CollegevilleUnited States - New York - New York CityWe're in relentless pursuit of breakthroughs that change patients' lives. We innovate every day to make the world a healthier place.
To fully realize Pfizer's purpose – Breakthroughs that change patients' lives – we have established a clear set of expectations regarding "what" we need to achieve for patients and "how" we will go about achieving those goals.
Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world.
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 include the design, development, and maintenance of clinical databases, ensuring the integrity of clinical data, and 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 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 to achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative team environment for your colleagues.
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 projects that may arise.Work 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.Comply with applicable SOPs and work practices.Develop knowledge of data capture tools and methods that support the accuracy and integrity of study data.Qualifications Must-Have Bachelor's 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 the 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 communication 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, 2024Work 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 - NOThe 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, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure.
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. This position requires permanent work authorization in the United States.
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