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Data Review Pharmacist Jobs (NOW HIRING)

... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...

... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...

... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...

... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...

... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...

Educational scientific background such as MD, PharmD, PhD, Nursing degree, MSc * ≥ 5 years of pharmaceutical clinical/medical data review experience is required, including clinical crosscheck ...

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Data Review Pharmacist information

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How much do data review pharmacist jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for data review pharmacist in the United States is $60.91, according to ZipRecruiter salary data. Most workers in this role earn between $56.01 and $67.31 per hour, depending on experience, location, and employer.

What is a data review pharmacist?

Data Review Pharmacists are licensed pharmacists who specialize in reviewing and validating medication-related data, often within clinical trials, pharmaceutical companies, or healthcare organizations. Their primary responsibilities include ensuring the accuracy, completeness, and compliance of pharmaceutical data, such as medication orders, clinical trial results, and patient safety reports. They play a critical role in maintaining regulatory standards, supporting quality assurance, and helping ensure patient safety by identifying discrepancies or potential medication errors in data sets.

What are the key skills and qualifications needed to thrive as a data review pharmacist?

To thrive as a Data Review Pharmacist, you need a solid background in pharmacy practice, drug information, and regulatory compliance, usually supported by a PharmD degree and pharmacist licensure. Familiarity with clinical data management systems, electronic health records (EHRs), and pharmacovigilance databases is essential. Strong attention to detail, analytical thinking, and effective communication skills make someone stand out in this role. These capabilities are crucial for ensuring medication safety, accurate data analysis, and compliance with healthcare regulations.

What are some common challenges faced by data review pharmacists, and how can they be addressed?

Data Review Pharmacists often encounter challenges such as managing large volumes of clinical or prescription data while ensuring accuracy and compliance with regulatory standards. Balancing attention to detail with efficiency is essential, as errors can impact patient safety or regulatory outcomes. To address these challenges, pharmacists typically leverage specialized software tools, develop strong organizational habits, and collaborate closely with clinical teams and IT specialists to clarify data discrepancies and maintain high-quality standards.

What does a data review pharmacist do?

A data review pharmacist evaluates medication data, prescription records, and clinical information to ensure accuracy, safety, and compliance with regulations. They analyze data to identify discrepancies, support medication therapy management, and collaborate with healthcare teams, often using specialized software and maintaining licensure requirements.

What are popular job titles related to Data Review Pharmacist jobs?

For Data Review Pharmacist jobs, the most frequently searched job titles are:

Infographic showing various Data Review Pharmacist job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 83% Full Time, 12% Part Time, and 3% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $126,701 per year, or $60.9 per hour.

Quality Assurance Data Review Scientist

High Point, NC • On-site

Cambrex
Pharmaceutical and Medicine Manufacturing • 1 - 5K employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Cambrex rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz


Job description

Company Information

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With over 40 years of experience and a growing team of over 2,200 experts servicing global clients from North America and European sites, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.

At Cambrex, our people set us apart. We're committed to attracting, nurturing, and retaining a passionate and talented team of valued experts in our fast-paced and growing company. We offer an exceptional benefits package including medical, dental, vision, Life, LTD, generous vacation in your first year, sick time, and retirement savings!

Known for our scientific and manufacturing excellence, as well as our strong customer focus, we offer a range of career opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world.

Overview:

Come join our QA team of experts.  The Data Review Scientist conducts data review activities for data generated by GMP Analytical for validation of analytical test methods, testing of cleaning samples, raw materials, process intermediates, final APIs, and final dosage forms, characterizing/qualifying Reference Standards, and Stability results. These data reviews are accomplished by review and approval of GMP Analytical Laboratory data located in notebooks, Material Release Forms, stability reports, methods qualifications/validations and reports, etc., as well as other documents as assigned.

Responsibilities:
  • Reviews chromatographic/other data and related notebooks as specified by Standard Operating Procedures (SOPs). Evaluates data to ensure compliance with analytical methods, client criteria, SOPs, and Good Manufacturing Practices (GMP).
  • Must be able to understand analytical data (chromatographic and other) and scrutinize routine and non-routine testing results to ensure compliance, accuracy, and completeness of work based on documented data.
  • Must be able to critically and in detailed fashion review/verify Reports, SOPs, Specifications, Analytical procedures, etc. Example: Reviews sample results tables and analytical reports for completeness and accurate representation of the data and report findings.
  • Must be able to solve practical problems and deal with a variety of concrete variables in situations where limited standardization exists.
  • Must be able to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
  • Organizes workflow and tasks to maximize efficiency (e.g., prioritize review/writing based on client/business needs, etc.).
  • Demonstrated ability to work with others at all levels of the organization and have basic knowledge of computers and industry-related software.
  • Ability to work effectively under pressure to meet deadlines.
  • Ensures compliance with company policies and SOPs as well as FDA and other applicable guidelines.
Qualifications / Skills:

Fundamental understanding (experience is not required) with the following analytical technologies:

  • Titrations (manual and automated)
  • Basic wet chemistry
  • FTIR
  • NMR
  • XRPD
  • DSC
  • HPLC
  • GC
  • MS
  • Working knowledge of other analytical equipment common to the pharmaceutical industry.
Education, Experience, and Licensing Requirements: (Text Only)- BS or MS in Chemistry (or closely related discipline). Relevant background in GXP/QC-compliant pharmaceutical laboratory environment. - Excellent verbal and written communication and interpersonal skills, problem-solving, and organizational skills. - Demonstrated ability to work in a diverse team environment. - Proficiency with Microsoft software (Word, Excel and PowerPoint). Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.   #LI-RD1Employment Type: FULL_TIME

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About Cambrex

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

East Rutherford, NJ, US

Year founded

1981

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