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Phd Drug Development Scientist Jobs in Reno, NV (NOW HIRING)

RXinsider LTD.

Metrology Technician I

Reno, NV · On-site

$71.64/hr

... development and safe manufacture of new drug therapies. When you join our family, you will have a ... Whether your background is in life sciences, finance, IT, sales or another area, your skills will ...

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Storm Staffing

R&D Engineering Manager

Carson City, NV · On-site

Bachelor's degree in Engineering, Materials Science, Chemistry, or related field (Master's or PhD preferred). * 8+ years of R&D experience in aerospace, advanced manufacturing, or related industries.

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Phd Drug Development Scientist information

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How much do phd drug development scientist jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for phd drug development scientist in Reno, NV is $38.55, according to ZipRecruiter salary data. Most workers in this role earn between $28.27 and $46.01 per hour, depending on experience, location, and employer.

What does a PhD drug development scientist do?

A PhD Drug Development Scientist is responsible for researching, designing, and conducting experiments to develop new pharmaceutical drugs or improve existing ones. They typically work in laboratories within pharmaceutical companies, biotechnology firms, or academic institutions. Their work involves understanding disease mechanisms, identifying drug targets, optimizing drug candidates, and ensuring safety and efficacy through preclinical and clinical trials. They also analyze data, collaborate with interdisciplinary teams, and comply with regulatory standards throughout the drug development process.

What are the key skills and qualifications needed to thrive as a PhD drug development scientist, and why are they important?

To thrive as a PhD Drug Development Scientist, you need deep expertise in pharmacology, biochemistry, and molecular biology, typically backed by a doctoral degree in a relevant scientific field. Familiarity with laboratory techniques, data analysis software, and regulatory documentation systems is crucial, as are certifications like Good Laboratory Practice (GLP) or Good Clinical Practice (GCP). Strong analytical thinking, meticulous attention to detail, and effective collaboration and communication skills help you navigate complex research and multidisciplinary teams. These skills ensure rigorous scientific discovery, regulatory compliance, and successful advancement of drug candidates from research through clinical development.

What are some common challenges faced by PhD drug development scientists during the transition from discovery to clinical trials?

PhD Drug Development Scientists often encounter challenges when moving a promising compound from the discovery phase to clinical trials, such as ensuring the drug's safety profile, scalability of synthesis, and regulatory compliance. Balancing scientific rigor with tight project timelines requires strong project management and cross-functional collaboration with regulatory, clinical, and manufacturing teams. Additionally, adapting to evolving regulatory requirements and troubleshooting unexpected preclinical results are common hurdles. Overcoming these challenges is crucial for advancing new therapies to patients and offers valuable experience for career growth.

What is the difference between Phd Drug Development Scientist vs Pharmacologist?

AspectPhd Drug Development ScientistPharmacologist
Required CredentialsPhD in Pharmacology, Chemistry, or related fieldPhD or MD in Pharmacology or related discipline
Work EnvironmentResearch labs, pharmaceutical companies, biotech firmsResearch institutions, pharmaceutical companies, healthcare settings
Industry UsageDeveloping new drugs, conducting preclinical studiesStudying drug effects, mechanisms, and interactions
Common Search/ComparisonYesYes

The Phd Drug Development Scientist focuses on designing and developing new drugs through research and preclinical testing, while the Pharmacologist studies how drugs work in the body, including their effects and interactions. Both roles require advanced degrees and are integral to the pharmaceutical industry, but they differ in their primary focus and daily responsibilities.

What are popular job titles related to Phd Drug Development Scientist jobs in Reno, NV?

For Phd Drug Development Scientist jobs in Reno, NV, the most frequently searched job titles are:

What job categories do people searching Phd Drug Development Scientist jobs in Reno, NV look for?

The top searched job categories for Phd Drug Development Scientist jobs in Reno, NV are:

Phd Drug Development Scientist jobs near you

Research Scientist I - Bioanalytical Science (Method Development/Validation)

Charles River Laboratories, Inc.

Reno, NV

$90K - $95K/yr

Full-time

Re-posted 25 days ago

Charles River Laboratories rating

8.4

Company rating: 8.4 out of 10

Based on 94 frontline employees who took The Breakroom Quiz

23rd of 86 rated pharmaceutical

Job description

For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Summary

We are seeking an experienced Research Scientist (Bioanalytical) for our Safety Assessment site located in Reno, NV. 

Serve as a scientist in the conduct of assigned preclinical and clinical research studies of basic to moderate complexity, to include study management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects.   

We are seeking a Research Scientist I (Bioanalytical) for our Safety Assessment site located in Reno, NV. 

This position will serve as a scientist in the conduct of assigned nonclinical and clinical bioanalytical studies at all levels of complexity, to include study management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects, as appropriate. Additional responsibilities include serving as a primary scientific contact for key clients and the on-site support of their programs, as well as the support of specialty studies.  The ideal candidate will have experience with design and optimization of ligand binding assays including ELISA, MSD, or Gyrolab platforms.   

•    Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline. Related Master's degree (M.S./M.A.) or PhD preferred.
•    Minimum of 3 to 5 years related experience in the contract research, academic, or pharmaceutical industry. 

•    An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•    Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate.
•    Effective written and verbal communication skills.
•    Ability to handle multiple projects, prioritize work and meet deadlines.
•    Proficiency in the use of standard software including Microsoft® Excel, Word, Powerpoint, etc. and with standard laboratory calculations.

The pay range for this position is $90,000 to $95,000 annually USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market.  Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.


About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 17,000 employees within 90 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of ~85% of the drugs approved by the FDA in 2019.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

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About Charles River

Sourced by ZipRecruiter

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947

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