ZipRecruiter

Log In

2

Full Time Preclinical Cro Jobs (NOW HIRING)

Neuralink

Preclinical Study Coordinator

Austin, TX · On-site

$31 - $53/hr

Background in a CRO or medical device preclinical setting. * Familiarity with electronic data ... Base Salary Range: $31-$53 USD What We Offer: Full-time employees are eligible for the following ...

Legend Biotech USA, Inc.

RequirementsR&D, Preclinical development, Clinical, CMC and regulatory MS/PhD/Pharm D in ... These benefits are offered exclusively to permanent full-time employees. Contractors are not ...

next page

Showing results 1-20

All JobsFull Time Preclinical Cro Jobs

Full Time Preclinical Cro information

See salary details

$16

$35

$62

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

As of Jun 13, 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:
Full Time Preclinical Cro jobs near you
Infographic showing various Full Time Preclinical Cro job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 84% Full Time, and 15% Part Time. Highlights an 74% Physical, 4% Hybrid, and 22% Remote job distribution, with an average salary of $72,895 per year, or $35 per hour.

Business Development Manager, ADME, DMPK, Toxicology Preclinical Research Services (Copy)

RPM ReSearch

Philadelphia, PA

$80K - $134K/yr

Full-time

Posted 20 days ago

Job description

City Region PA, NJ, MD


Territory Covered- East Coast


Job Title Director of Business Development (IC) Drug Development Services


5-6 products sold

-Bioanalytical Service

-ADME/DMPK Services

-Toxicology Services

-Pre Clinical Drug Development Services

-Drug Delivery Testing Services


Base Range- Total Comp Range

$80,000-90,000 Base On Target Earnings $125,000 Base increase commensurate with CRO Service Sales Experience.


Role-

Business Development and Growth of PreClinical Services.


Overview:

Rapidly Growing mid-size Preclinical Contract Research Organization (CRO) is expanding its West Coast Territory with another Director of BD to support continued growth. Productive territory is handled by inside sales and is ready for full-time Business Development. Internal Scientific Experience is available. Ultimate decision-making capabilities will remain with the Director of Business Development. Support and promote Pre-Clinical Drug Development Services by identifying, developing, managing, and retaining potential and existing accounts within the West Coast Territory.


Client Attributes:

  • Unique efficacy models that the big players don’t have

  • Nimble and able to shift in response to client’s needs

  • The ability for custom services that are not out of a box

  • Research facility with unique model generation capabilities.

  • Over 25 years experience in the market.


Responsibilities:

• Identify opportunities to coordinate client contact with Government agencies, biotech/pharmaceutical companies (both prospective and current clients of Company), to market and ensure customer satisfaction with Company services.

• Respond to client inquiries and provide information including cost estimates and timelines in response to inquiries

• Write routine reports and correspondence in a professional manner

• Manage multiple opportunities and projects simultaneously

• Possess the capacity to advocate on the client's behalf

• Visit prospective clients and present information regarding the preclinical and clinical capabilities of the company to obtain new business.

• Coordinate appointments with clients as needed to expand the growth of the business

• Identify prospective clients and convert.

• Book local events to present company information and generate contacts for prospective businesses.

• Partner with clients and in-house scientific experts to recommend solutions to a wide range of pre-clinical study design challenges.

• Coordinate internal project teams to support client requests and anticipated business needs.

• Contribute to developing and executing strategies that will increase the efficiency of the Client Services group by working with fellow group members as a team.


Qualifications:

  • BS or MS with 6-10 years related experience and/or training in the biotech, pharmaceutical development or preclinical CRO industry

  • Mandatory 3-8 years experience in Business Development in a technical area

  • Solid knowledge of the CRO and/or Biotech and Pharmaceutical industries with a firm grasp on preclinical toxicology, both GLP and non-GLP studies.

  • Demonstrates success in managing multiple projects and opportunities simultaneously.