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Pharmaceutical Research Analyst Jobs (NOW HIRING)

Jr. Operations Research Analyst

Huntsville, AL · On-site

$97K - $114K/yr

... pharmaceutical research. We are looking for individuals who thrive on making an impact and want the ... The OR Analyst will conduct analyses of expeditionary medical systems and assist in the development ...

Jr. Operations Research Analyst

Huntsville, AL · On-site

$97K - $114K/yr

... pharmaceutical research. We are looking for individuals who thrive on making an impact and want the ... The OR Analyst will conduct analyses of expeditionary medical systems and assist in the development ...

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... Labcorp is seeking a Research Analyst - QWBA to join our metabolism team, in Madison, WI. Work ...

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... Labcorp is seeking a Research Analyst - QWBA to join our metabolism team, in Madison, WI. Work ...

Showing results 21-40

Pharmaceutical Research Analyst information

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$38.5K

$74K

$99.5K

How much do pharmaceutical research analyst jobs pay per year?

As of Sep 9, 2026, the average yearly pay for pharmaceutical research analyst in the United States is $73,965.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,000.00 and $98,500.00 per year, depending on experience, location, and employer.

What does a pharmaceutical research analyst do?

A Pharmaceutical Research Analyst is responsible for collecting, analyzing, and interpreting data related to pharmaceutical products, including clinical trials, market trends, and regulatory information. They help pharmaceutical companies make evidence-based decisions regarding drug development, pricing, and marketing strategies. Their work ensures that new medications are both effective and safe for public use, while also helping companies stay competitive and compliant with regulations.

What are some typical challenges pharmaceutical research analysts face when working on new drug development projects?

Pharmaceutical Research Analysts often encounter challenges such as interpreting complex clinical data, managing large datasets, and keeping up with rapidly evolving regulatory requirements. Coordinating with cross-functional teams—including scientists, regulatory affairs, and marketing—can also require strong communication and project management skills. Staying current with scientific literature and ensuring data integrity throughout the research process are crucial for success in this role.

What are the key skills and qualifications needed to thrive as a pharmaceutical research analyst, and why are they important?

To thrive as a Pharmaceutical Research Analyst, you need a strong background in pharmaceutical sciences, data analysis, and research methodologies, often supported by a relevant degree in pharmacy, chemistry, or life sciences. Familiarity with statistical software (such as SAS, SPSS, or R), laboratory information management systems (LIMS), and regulatory guidelines like GCP is essential. Critical thinking, attention to detail, and strong written and verbal communication skills help analysts interpret complex data and present findings effectively. These competencies ensure rigorous, accurate research that supports drug development and regulatory compliance in a highly regulated industry.

What is the difference between Pharmaceutical Research Analyst vs Pharmaceutical Data Analyst?

AspectPharmaceutical Research AnalystPharmaceutical Data Analyst
Required CredentialsBachelor's degree in life sciences, pharmacy, or related field; often some research experienceBachelor's degree in data science, statistics, or related field; proficiency in data analysis tools
Work EnvironmentResearch labs, pharmaceutical companies, clinical trial settingsData centers, pharmaceutical companies, healthcare analytics teams
Employer & Industry UsageUsed in R&D, clinical trials, regulatory submissionsUsed in data analysis, reporting, and decision-making processes

The main difference is that Pharmaceutical Research Analysts focus on conducting research, clinical trials, and scientific analysis, while Pharmaceutical Data Analysts specialize in analyzing data sets to inform business and clinical decisions. Both roles require analytical skills but differ in their core activities and tools used.

How do I become a pharmaceutical research analyst?

To become a pharmaceutical research analyst, typically a bachelor's degree in pharmacy, biology, chemistry, or a related field is required, often followed by experience in clinical research or data analysis. Developing skills in data management, statistical software, and understanding regulatory guidelines can enhance job prospects; some roles may require advanced degrees or certifications such as RAC or SAS certification.
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Cities with the most Pharmaceutical Research Analyst job openings:

What states have the most Pharmaceutical Research Analyst jobs?

States with the most job openings for Pharmaceutical Research Analyst jobs include:

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Infographic showing various Pharmaceutical Research Analyst job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 88% Full Time, 9% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $73,965 per year, or $35.6 per hour.

Senior Device Engineer, Pharmaceutical R&D

Weston, FL • On-site

Transpire BIO Inc.
Biotechnology Research and Development • 11 - 50 employees

$99K - $136K/yr

Full-time

Re-posted 28 days ago


Job description

Position Summary

The Senior Device Engineer is responsible for device engineering activities in the context of pharmaceutical research and development (R&D). The device mechanical engineer will be responsible for early to late-stage device development activities and commercialization of drug-device combination products. The Device engineer will be responsible for design, prototyping, technical analysis, and testing of orally inhaled and nasal drug products (OINDPs). Provide device engineering leadership in the direction, initiation, planning, coordination, implementation, execution, control, and completion of specific device project(s) ensuring consistency with organizational strategy, commitments, and goals. The device engineer will need to ensure that the device designs meet user needs, regulatory and quality requirements, and consider manufacturability. This is a hands-on position which requires daily tactical responsibilities leading up to strategic decisions.

Essential Duties and Responsibilities

  • In support of the Product Development Teams, provide technical leadership in the device development area.
  • Execute design and development of orally inhaled and nasal drug products (OINDPs) following design controls.
  • Lead and execute analysis for device and product characterization, design feasibility, and design verification.
  • Lead and execute technical analyses including statistical analysis and tolerance analysis.
  • Lead root cause investigations.
  • Support scale-up and commercialization efforts.
  • Document studies and author documents per US FDA, EMA, MHRA and other global health authority requirements.
  • Interface and lead activities with third party contract research, development, and manufacturing organizations.
  • Contribute towards and maintain device design history files (DHF).
  • Document standard operating procedures (SOPs) for design controls in the context of pharmaceutical drug-device combination products.
  • Provide project updates/reporting through program governance.
  • Provide leadership and support for inter-site best practices (technology transfer, process validation, etc.) and phase appropriate guidelines and policies.
  • Execute project strategy, priorities, and milestones ensuring visibility and accountability.
  • Proactively lead with integrity and engage cross functional project teams and stakeholders.
  • Support organizational / departmental initiatives.
  • Prepare and conduct presentations to all levels of the organization which may include project technical and budgetary information.

Required Qualifications

  • A M.S, in Mechanical Engineering, Electrical Engineering, Material Sciences or related discipline with 7 to 10 years, B.S. with 10 to 14 years device development experience in pharmaceutical or related field.
  • Experience with device development in the context of pharmaceutical R&D and product development is a must to have.
  • Must possess expert knowledge of mechanical design with preference for SolidWorks.
  • Must possess expert knowledge of tools to conduct statistical and tolerance analysis.
  • Must possess knowledge of manufacturing processes including injection molding and metal machining processes.
  • Must possess knowledge of regulations and standards including US 21 CFR Part 820, ISO 13485, ISO 14971, ISO 10993, EU MDR etc.
  • Experience with device assembly processes including manual, semi-automated and/or commercial scale automated processes is a plus.
  • Experience in development of orally inhaled and nasal drug products (OINDPs) is a plus.
  • Experience in mold tool design, optimization and qualification is a plus to have.
  • Experience with Notified Bodies and CE marking is a plus.
  • Strong English language skills including writing ability and oral communication.
  • Demonstrates good judgment as well as cultural, social, and environmental awareness.

Preferred Qualifications

  • Experience in a regulated laboratory (pharma, biotech, medical device, mechanical, or environmental)
  • Knowledge of GMP, GLP, or ISO standards

Why Join Us?

We are a fast-growing pharmaceutical startup dedicated to innovation and improving patient outcomes. Join us to gain hands-on experience in a growing pharmaceutical business, get exposure to various functions with opportunities for career development and work in a collaborative and supportive work environment.