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Full Time Preclinical Cro Jobs (NOW HIRING)

... CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 ... Key Responsibilities * Assist in developing analytical methods to support sponsor preclinical PK ...

... Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research ... Perform routine bioanalysis of preclinical and clinical samples under GLP and non-GLP conditions.

Administrative Assistant

Brookings, SD · On-site

$16.50 - $22.25/hr

Administrative Assistant | Clinvet South Dakota | Full-Time Our Story Clinvet South Dakota is a global veterinary contract research organization (CRO) that conducts preclinical and clinical trials to ...

Administrative Assistant

Brookings, SD

$16.50 - $22.25/hr

Administrative Assistant | Clinvet South Dakota | Full-Time Our Story Clinvet South Dakota is a global veterinary contract research organization (CRO) that conducts preclinical and clinical trials to ...

SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and ... This position is full-time onsite and can work out of our Redmond, WA or Princeton, NJ locations.

Animal Research Technician

Waverly, NY · On-site

$18 - $22/hr

... organization (CRO), specializing in in vitro, preclinical, and clinical trials to evaluate the ... * Full-time, 40 hours per week * Typical schedule: 7:00 AM - 3:30 PM * Weekend, holiday, and ...

Animal Research Technician

Waverly, NY · On-site

$18 - $22/hr

... organization (CRO), specializing in in vitro, preclinical, and clinical trials to evaluate the ... * Full-time, 40 hours per week * Typical schedule: 7:00 AM - 3:30 PM * Weekend, holiday, and ...

... organization (CRO) specializing in in-vitro, preclinical, and clinical trials to evaluate the ... Must be fit for duty and able to work safely Schedule & Work Environment * Full-time, 40 hours per ...

... organization (CRO) specializing in in-vitro, preclinical, and clinical trials to evaluate the ... Must be fit for duty and able to work safely Schedule & Work Environment * Full-time, 40 hours per ...

... organization (CRO) specializing in in vitro, preclinical, and clinical trials to evaluate the ... * Full-time, 40 hours per week * Typical schedule: 7:00 AM - 3:30 PM * Weekend, holiday, and ...

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Full Time Preclinical Cro information

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$16

$35

$62

How much do full time preclinical cro jobs pay per hour?

As of Jul 29, 2026, the average hourly pay for full time preclinical cro in the United States is $35.05, according to ZipRecruiter salary data. Most workers in this role earn between $25.48 and $41.59 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Full-Time Preclinical CRO (Contract Research Organization) professional, and why are they important?

To thrive as a Full-Time Preclinical CRO professional, you need a solid background in biological sciences or pharmacology, with at least a bachelor’s or master’s degree and experience in laboratory research. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP) standards, and data analysis tools like GraphPad Prism is typically required. Strong attention to detail, effective communication, and problem-solving abilities are crucial soft skills for this role. These competencies ensure the accuracy, reliability, and regulatory compliance of preclinical studies, which are foundational for successful drug development.

What are full-time preclinical CRO jobs?

Full-time preclinical CRO (Contract Research Organization) jobs involve working for organizations that provide research services to pharmaceutical, biotechnology, and medical device companies before clinical trials begin in humans. These roles typically include conducting laboratory experiments, animal studies, data analysis, and reporting to help assess the safety and efficacy of new drugs or treatments. Employees in these positions may work as scientists, technicians, project managers, or quality assurance specialists. The work is essential in supporting drug development pipelines and ensuring regulatory compliance.

What is the difference between Full Time Preclinical Cro vs Full Time Preclinical Study Coordinator?

AspectFull Time Preclinical CroFull Time Preclinical Study Coordinator
CredentialsTypically requires advanced degrees in life sciences, experience in CRO settingsRequires bachelor's or master's in related fields, some experience in clinical or preclinical studies
Work EnvironmentWorks within CROs, managing multiple client projects, regulatory complianceWorks in research labs or clinical settings, coordinating study activities and documentation
Employer & Industry UsagePrimarily employed by Contract Research Organizations in pharma/biotechEmployed by research institutions, biotech companies, or CROs

While both roles are involved in preclinical research, a Full Time Preclinical Cro focuses on managing and overseeing preclinical studies within a CRO environment, often requiring more advanced scientific credentials. A Full Time Preclinical Study Coordinator typically handles the day-to-day coordination of preclinical studies, ensuring protocols are followed and documentation is maintained. Both roles are essential in the drug development process but differ in scope and responsibilities.

What are some typical challenges faced by professionals working full-time at a preclinical CRO, and how can new hires effectively navigate them?

Working full-time at a preclinical Contract Research Organization (CRO) often involves managing multiple projects with tight deadlines and adapting to shifting client requirements. New hires may find it challenging to balance regulatory compliance with the fast-paced nature of the work. To succeed, it's important to develop strong organizational skills, communicate proactively with cross-functional teams, and stay updated on industry guidelines. Building relationships with experienced colleagues can also provide valuable support and insights as you adjust to the CRO environment.
More about Full Time Preclinical Cro jobs
What are the most commonly searched types of Preclinical Cro jobs? The most popular types of Preclinical Cro jobs are:
What job categories do people searching Full Time Preclinical Cro jobs look for? The top searched job categories for Full Time Preclinical Cro jobs are:
Infographic showing various Full Time Preclinical Cro job openings in the United States as of July 2026, with employment types broken down into 23% Locum Tenens, 69% Full Time, 3% Part Time, 2% Contract, and 3% Summer. Highlights an 75% Physical, 3% Hybrid, and 22% Remote job distribution, with an average salary of $72,895 per year, or $35 per hour.

$48K - $55K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 28 days ago


Job description

Associate Scientist

Location

Exton, PA (onsite)

Salary Range: $48,000-55,000

About Pharmaron

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.

We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit www.pharmaron.com.

Launch Your Career in Drug Discovery

Are you an early-career scientist looking to make an impact in pharmaceutical research? We are seeking an Associate Scientist to join our Bioanalytical Sciences team, supporting discovery bioanalysis and preclinical pharmacokinetic (PK) studies. In this role, you'll work alongside experienced scientists using advanced analytical techniques to generate high-quality data that supports drug discovery and development.

This is an excellent opportunity for someone with laboratory experience who is passionate about analytical science, enjoys hands-on work, and thrives in a collaborative research environment.

What You'll Do

As an Associate Scientist, you'll play a key role in the successful execution of bioanalytical studies while maintaining the highest standards of quality and scientific integrity.

Key Responsibilities

  • Assist in developing analytical methods to support sponsor preclinical PK studies.
  • Prepare biological samples for bioanalytical testing and analysis.
  • Perform laboratory studies in accordance with approved study protocols and scientific plans.
  • Process, analyze, and document study results with exceptional accuracy and attention to detail.
  • Generate technical reports and maintain complete study documentation.
  • Perform routine maintenance and troubleshooting of laboratory instrumentation.
  • Maintain laboratory organization and ensure compliance with Standard Operating Procedures (SOPs).
  • Stay current with scientific advancements and emerging analytical technologies.
  • Collaborate with scientists and cross-functional teams to ensure timely delivery of high-quality client results.
  • Support additional laboratory projects and assignments as needed.

Qualifications

Required

  • Bachelor's degree in Pharmaceutical Sciences, Life Sciences, Chemistry, Biochemistry, or a related scientific discipline.
  • Minimum of one year of laboratory experience in bioanalytical testing, pharmaceutical research, or a related environment.
  • Experience with HPLC and/or UHPLC-MS instrumentation.
  • Strong organizational skills with exceptional attention to detail.
  • Ability to accurately document, analyze, and report scientific data.
  • Strong work ethic with the ability to thrive in a fast-paced, team-oriented laboratory.

Preferred

  • Experience with Agilent or Waters LC-MS/MS systems.
  • Experience performing noncompartmental pharmacokinetic analysis using Phoenix WinNonlin.
  • Knowledge of additional chromatographic techniques and conventional HPLC analytical methods.
  • Experience supporting preclinical pharmacokinetic (PK) or drug metabolism and pharmacokinetics (DMPK) studies.

What Makes You Successful

You are someone who:

  • Is passionate about scientific research and analytical problem-solving.
  • Maintains exceptional attention to detail and data quality.
  • Learns quickly and adapts to new laboratory methods and technologies.
  • Works effectively both independently and within collaborative scientific teams.
  • Demonstrates strong organizational and time-management skills.
  • Takes pride in producing accurate, reliable results for clients.

Work Environment

  • Full-time, on-site laboratory position.
  • Combination of laboratory and office work.
  • Ability to stand or sit for extended periods throughout the workday.
  • Ability to lift up to 15 pounds.
  • Frequent use of laboratory instrumentation, computers, and scientific equipment.
  • Work performed in laboratory environments with varying temperatures, lighting, and noise levels.

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:

  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

How to Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.

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