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Preclinical Cro Jobs (NOW HIRING)

Pharmaron

In Vivo Operations Specialist

Carlsbad, CA · On-site

$80K - $100K/yr

Experience in laboratory, preclinical, CRO, or vivarium environments * Experience coordinating operations or projects in fast-paced settings * Strong organizational and communication skills

Pharmaron

In Vivo Operations Specialist

Carlsbad, CA

$80K - $100K/yr

Experience in laboratory, preclinical, CRO, or vivarium environments * Experience coordinating operations or projects in fast-paced settings * Strong organizational and communication skills

Neuralink

Preclinical Study Coordinator

Austin, TX · On-site

$31 - $53/hr

Background in a CRO or medical device preclinical setting. * Familiarity with electronic data capture systems or GLP-compliant documentation platforms. Additional Requirements and Competencies:

Integrated Resources INC

Perform an inventory review for incoming CRO clinical study files; receive, index, and file preclinical study records; responsible for offsite archival of documents; participate in periodic file room ...

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$44K

$103.2K

$239.5K

How much do preclinical cro jobs pay per year?

As of Jun 15, 2026, the average yearly pay for preclinical cro in the United States is $103,249.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,000.00 and $200,000.00 per year, depending on experience, location, and employer.

What are the typical career advancement opportunities for someone working in a Preclinical CRO role?

Professionals in Preclinical CRO roles can advance their careers by moving into senior scientist, project management, or team leadership positions, often taking on greater responsibility for study design and client management. With experience, it's also common to specialize in specific therapeutic areas or regulatory submission processes, or to progress to roles overseeing entire departments or business units. Many CROs offer ongoing training and development, enabling professionals to stay current with industry trends and broaden their expertise. Advancement often depends on demonstrated leadership, technical excellence, and a strong track record in delivering high-quality, compliant results. This environment rewards proactive learning and collaboration, providing ample opportunities for long-term career growth.

What is a Preclinical CRO job?

A Preclinical CRO (Contract Research Organization) job involves supporting pharmaceutical and biotechnology companies in conducting preclinical research before human trials. Professionals in this role assist with study design, laboratory testing, regulatory compliance, and data analysis to evaluate the safety and efficacy of drug candidates. They work with scientists and researchers to conduct in vitro and in vivo studies, ensuring high-quality results that meet regulatory standards. Preclinical CRO employees may specialize in toxicology, pharmacokinetics, bioanalysis, or other key areas that contribute to drug development.

What are the key skills and qualifications needed to thrive in the Preclinical Cro position, and why are they important?

To thrive as a Preclinical CRO (Contract Research Organization) professional, you need a solid background in life sciences or pharmacology, experience in laboratory research, and a strong understanding of regulatory compliance in drug development. Expertise with laboratory information management systems (LIMS), data analysis tools, and familiarity with GLP (Good Laboratory Practice) certification are typically important. Strong attention to detail, project management skills, and effective communication are valuable soft skills for success in this role. These competencies ensure accurate preclinical study execution, compliance with regulatory standards, and effective collaboration within multidisciplinary teams.

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Preclinical Cro jobs near you
Infographic showing various Preclinical Cro job openings in the United States as of June 2026, with employment types broken down into 97% Full Time, and 3% Part Time. Highlights an 74% Physical, 4% Hybrid, and 22% Remote job distribution, with an average salary of $103,249 per year, or $49.6 per hour.
Executive Director, DMPK

Executive Director, DMPK

Frontage Laboratories

Exton, PA • On-site

Full-time

Posted 23 days ago

Job description

Title: Executive Director, DMPK

Location: Exton, PA

Reports to: VP, DMPK

Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China, and growing over 30% YOY. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Position/Job Summary:

The successful candidate will lead the in vitro ADME and pharmacokinetic functions of the DMPK department at the Exton, PA site. The position involves overseeing a group of approximately 20 scientists performing studies to evaluate the pharmacokinetics, drug metabolism and drug-drug interaction potential of development and discovery-stage drugs.

The successful candidate will be responsible for setting performance and financial goals for the business unit and ensuring the required resources/personnel are in place to achieve the goals.

Roles & Responsibilities:

  • Keep abreast of new scientific developments and regulatory requirements and ensure the work within the group is performed accordingly
  • Have a general strategy of soliciting business, meet customers and provide scientific input so that the right studies are performed to address the scientific and/or regulatory question at hand
  • Design studies as needed and include in study proposals /protocols
  • Prepare study proposals at the request of customers
  • Provide guidance in the preparation of study protocols for in vitro and in vivo studies
  • Help with the interpretation of data and conclusions/summaries for completed studies
  • Ensure that all studies are conducted efficiently and in a timely manner while maintaining highest quality of data
  • Ensure that the scientists follow Frontage SOPs, DMPK guidelines, and study protocols while conducting studies
  • Other duties as assigned

Education, Experience & Skills Required:

  • PhD in chemistry, biology, or related area
  • More than 10 years of related experience in the biotech, pharma or preclinical CRO industry
  • Solid knowledge of in vitro DMPK, drug transporters, enzyme kinetics and pharmacokinetics
  • Familiarity with bioanalysis using LC/MS/MS
  • Experience with drug discovery and development and the toxicology, drug metabolism, and pharmacokinetics data required at various stages of the drug discovery and development process
  • Good track record in leading small to large DMPK groups

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.