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Pfizer Data Scientist Jobs in Basking Ridge, NJ (NOW HIRING)

You may participate in the company group medical insurance plan Safety Data Management Specialist ... Consistently apply regulatory requirements and Pfizer policies Participate, as appropriate, in ...

Head of AI Clinical Excellence

New York, NY · On-site

$87K - $119K/yr

Partner with digital, data science, and technology teams to design, build, validate, and deploy AI ... Pfizer compensation structures and benefit packages are aligned based on the location of hire. The ...

Director, AI Product / Program Delivery

New York, NY · Hybrid

$254K - $266K/yr

As part of how Pfizer turns its AI ambition into delivered outcomes, you create the operational ... Experience with Medical Science Liaison (MSL) and Field Medical workflows * Experience translating ...

Showing results 41-60

Pfizer Data Scientist information

See Basking Ridge, NJ salary details

$38.6K

$126.5K

$202.5K

How much do pfizer data scientist jobs pay per year?

As of Aug 22, 2026, the average yearly pay for pfizer data scientist in Basking Ridge, NJ is $126,489.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,500.00 and $140,200.00 per year, depending on experience, location, and employer.

What is a Pfizer data scientist?

A Pfizer Data Scientist analyzes large datasets to extract insights that drive pharmaceutical research, drug development, and business strategies. They work with machine learning, statistical modeling, and data visualization to support decision-making in areas like clinical trials, drug safety, and patient outcomes. Collaboration with cross-functional teams, including researchers, engineers, and healthcare professionals, is a key part of the role. Strong skills in programming, data wrangling, and domain knowledge in life sciences or healthcare analytics are often required.

What types of projects does a Pfizer data scientist typically work on, and how does this impact collaboration with other teams?

Pfizer Data Scientists are often involved in projects related to drug discovery, clinical trial data analysis, patient outcome modeling, and real-world evidence generation. These projects require frequent collaboration with multidisciplinary teams including researchers, clinicians, biostatisticians, and IT professionals to ensure data-driven solutions support strategic business and research goals. Data Scientists participate in regular cross-functional meetings, contribute to study design, and help translate scientific questions into analytical models. This collaborative environment fosters continuous learning and enables professionals to see the impact of their work on advancing healthcare outcomes.

What are the key skills and qualifications needed to thrive as a Pfizer data scientist, and why are they important?

To thrive as a Pfizer Data Scientist, you need a solid background in statistics, programming (such as Python or R), machine learning, and a relevant degree in data science, computer science, bioinformatics, or a related field. Familiarity with data visualization tools (like Tableau), cloud platforms, and certifications in data analytics or related specializations are commonly required. Strong problem-solving, collaborative teamwork, and excellent communication skills are essential for effectively sharing insights with both technical and non-technical stakeholders. These skills are crucial for transforming complex biological and clinical data into actionable insights that drive research and innovation at Pfizer.

What are popular job titles related to Pfizer Data Scientist jobs in Basking Ridge, NJ?

For Pfizer Data Scientist jobs in Basking Ridge, NJ, the most frequently searched job titles are:

What job categories do people searching Pfizer Data Scientist jobs in Basking Ridge, NJ look for?

The top searched job categories for Pfizer Data Scientist jobs in Basking Ridge, NJ are:

Infographic showing various Pfizer Data Scientist job openings in Basking Ridge, NJ as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, and 4% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $126,489 per year, or $60.8 per hour.

Drug Safety Data Management Specialist

Global Pharmatek

Piscataway, NJ • On-site

Contractor

Re-posted 20 days ago


Job description

Company Description
We are proud to be part of the most precious thing on Earth: human life. Applying the technological expertise to the medical knowledge to derive near infallible results comes naturally to Global Pharma Tek, LLC. Global Pharma Tek is a fast-growing premier global pharmaceutical company that provides end-to-end services in pharmaceutical industry round the globe. Global Pharma Tek offers services like Drug Discovery, Clinical Trials, Drug Delivery, Regulatory and Intellectual Property Rights, Marketing and Strategic Human Resourcing. Global Pharma Tek is specialized in providing highly technical pharmaceutical and healthcare solutions and services in a cost effective way around the globe.
We are enterprise-class clinical software and clinical functional services provider, offers unique blend of both clinical trial domain and core IT expertise with thorough understanding of healthcare and pharma industry and regulatory standards. Global Pharma Tek, clinical functional services practice (FSP) enable pharmaceutical and life sciences industry customers realize their vision of safe, effective, and FDA approved delivery of drug at the lowest cost and at the fastest time to market.
With core technology focus in the areas of statistical programming, business intelligence & data warehousing, enterprise application integration and enterprise architecture development, enterprise resource planning and custom applications development, along with clinical domain expertise, Global Pharma Tek offers a full range of specialized functional clinical & IT in-sourcing, IT projects development, clinical functional & IT projects outsourcing, software enabled services.
Job Description
Job Description:
  • Enter applicable information into the global safety database for initial or follow up cases received via paper, fax or email.
  • Book-in, quality check and initially assess cases from suppliers sending cases to DSS via paper, email or fax.
  • Accept E2B cases received through the Argus Electronic Submissions Module (ESM) from European Health Authorities on behalf of Pfizer Country Offices that are not online with Argus and other submitters as necessary.
  • Monitor electronic mailboxes and Argus ESM to ensure timely acceptance of Adverse Event (AE) Reports Perform data entry into databases, as needed.
  • Ensure proper coding of events and drugs for cases to ensure correct forwarding to the relevant Therapeutic Area Teams and Licensing Group.
  • Upload AE reports to the Drop in Data Entry II application on behalf of country offices cannot on their own.

Qualifications
BA degree required with 1-3 years of Safety/ Pharmacovigilance Data experience. Argus experience.
Additional Information
All your information will be kept confidential according to EEO guidelines.

Global Pharmatek logo

About Global Pharmatek

Sourced by ZipRecruiter

Global Pharmatek is a leading Contract Research Organization (CRO) and integrated drug discovery solutions provider in the pharmaceutical industry. The company is located in Edison, New Jersey, USA. Their comprehensive range of services includes Drug Discovery, Clinical Trials, Regulatory Affairs, and Biometrics, designed with the goal of swiftly translating scientific innovation into a novel product. Founded with an unwavering commitment to enhance health and well-being worldwide, this leading-edge company lays emphasis on the highest quality standards, efficient delivery, and transparency.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

2011