Similar Jobs at Pfizer
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
The role involves creating engaging digital and print designs for medical communications, managing projects, and ensuring compliance with regulatory standards.
Top Skills:
Adobe Creative SuiteAICorel DrawIllustratorIndesignPowerPoint
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
The Data Manager supervises clinical trials, ensuring quality data management, review, query management, and compliance with data standards and SOPs.
Top Skills:
Edc System
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
As a Platform Engineer, you will develop and manage the enterprise pro-code AI Agent Platform using Azure, ensuring security, compliance, and robust operations. You'll automate cloud infrastructure, implement observability, and integrate AI services while collaborating across teams.
Top Skills:
Agent 365Azure Api ManagementAzure Data FactoryAzure DevopsBashCi/CdData LakeDatabricksDataikuFoundryGithub ActionsLangchainLanggraphAzurePythonSnowflakeTerraform
A productive, hands on programmer who applies technical knowledge and practical experience to deliver statistical programming deliverables to support assets and study teams with limited supervision early in role and independently later in role. •
Ensures excellence in th e programming of analysis ready datasets, tables, listings, and figures for which they are responsible •
Ensures adherence to high quality programming standards in their daily work. Accountable for the quality and timely delivery of datasets and displays required for their clinical study reports as well as other asset level deliverables they may be programming.
Ensures appropriate documentation and QC across the lifespan of the study for all of their programming deliverables.
Exhibi ts routine and occasionally complex problem solving skills, seeking direction when appropriate. •
Works with statisticians and programming leads to ensure clear specifications for their programmed deliverables are in place.
Will be knowledgeable in core safe ty standards as well as TA standards pertinent to their project, may aid in development of standards necessary for their study
May contribute to department level initiatives.
QUALIFICATIONS
Bachelor or Master (prefer red) Degree in Statistics, Biological Sciences, IT, or related field. •
At least 3 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency. •
Statistical Programming and SAS hand - on experience •
Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data. •
Good understanding of ICH and regulatory guidelines •
Working knowledge of clinical data and relevant data standards
Work Location Assignment: Flexible
Work Location Assignment: Hybrid
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
#LI-PFE
Ensures excellence in th e programming of analysis ready datasets, tables, listings, and figures for which they are responsible •
Ensures adherence to high quality programming standards in their daily work. Accountable for the quality and timely delivery of datasets and displays required for their clinical study reports as well as other asset level deliverables they may be programming.
Ensures appropriate documentation and QC across the lifespan of the study for all of their programming deliverables.
Exhibi ts routine and occasionally complex problem solving skills, seeking direction when appropriate. •
Works with statisticians and programming leads to ensure clear specifications for their programmed deliverables are in place.
Will be knowledgeable in core safe ty standards as well as TA standards pertinent to their project, may aid in development of standards necessary for their study
May contribute to department level initiatives.
QUALIFICATIONS
Bachelor or Master (prefer red) Degree in Statistics, Biological Sciences, IT, or related field. •
At least 3 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency. •
Statistical Programming and SAS hand - on experience •
Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data. •
Good understanding of ICH and regulatory guidelines •
Working knowledge of clinical data and relevant data standards
Work Location Assignment: Flexible
Work Location Assignment: Hybrid
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
#LI-PFE
Pfizer Chennai, Tamil Nadu, IND Office
Chennai, India
What you need to know about the Chennai Tech Scene
To locals, it's no secret that South India is leading the charge in big data infrastructure. While the environmental impact of data centers has long been a concern, emerging hubs like Chennai are favored by companies seeking ready access to renewable energy resources, which provide more sustainable and cost-effective solutions. As a result, Chennai, along with neighboring Bengaluru and Hyderabad, is poised for significant growth, with a projected 65 percent increase in data center capacity over the next decade.
