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Contract Research Organization Jobs (NOW HIRING)

RPM ReSearch

$7M/yr

... contract research organization that assists pharmaceutical and biopharmaceutical companies in identifying and overcoming research barriers in the development of cell and gene therapies. The client ...

Medpace

SAS Programmer - Experienced

Cincinnati, OH · On-site

Medpace is a full-service clinical contract research organization (CRO) that provides clinical development services to the biotechnology, pharmaceutical, and medical device industries. They are ...

Medpace

SAS Programmer - Entry Level

Cincinnati, OH · On-site

Medpace is a full-service clinical contract research organization that provides Phase I-IV clinical development services. They are seeking an Entry Level SAS Programmer to join their Biostatistics ...

Medpace, Inc.

Contract Manager

Cincinnati, OH · On-site

$85K - $114K/yr

Travel : minimal Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...

Medpace, Inc.

Contract Manager

Cincinnati, OH

$85K - $114K/yr

Travel : minimal Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...

Clingroup

Animal Research Technician

Waverly, NY · On-site

$18 - $22/hr

Animal Research Technician Clinvet NY - Waverly, NY About Us Clinvet NY is a global veterinary contract research organization (CRO), specializing in in vitro, preclinical, and clinical trials to ...

Clingroup

Animal Research Technician

Waverly, NY

$18 - $22/hr

Animal Research Technician Clinvet NY - Waverly, NY About Us Clinvet NY is a global veterinary contract research organization (CRO), specializing in in vitro, preclinical, and clinical trials to ...

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All JobsContract Research Organization Jobs

Contract Research Organization information

See salary details

$22.5K

$149.8K

$400K

How much do contract research organization jobs pay per year?

As of Jun 10, 2026, the average yearly pay for contract research organization in the United States is $149,808.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,500.00 and $224,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in a Contract Research Organization (CRO) role, and why are they important?

To excel in a Contract Research Organization (CRO), professionals typically need a background in life sciences or related fields, along with experience in clinical research processes and regulatory compliance. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are highly valued. Strong attention to detail, effective communication, and organizational skills distinguish top performers in CRO environments. These abilities are crucial for ensuring the accuracy, efficiency, and regulatory adherence of clinical trials conducted on behalf of sponsors.

What are some common challenges faced when working at a Contract Research Organization (CRO)?

Working at a Contract Research Organization can be highly rewarding, but it comes with unique challenges such as managing multiple client projects simultaneously, adapting to rapidly changing study protocols, and ensuring compliance with diverse regulatory requirements. CRO professionals often need to be flexible, detail-oriented, and comfortable with tight deadlines. Team collaboration is essential, as you’ll frequently work with cross-functional groups including clinical operations, data management, and regulatory affairs. Successfully navigating these challenges can lead to valuable experience and advancement opportunities within the industry.

What is the difference between Contract Research Organization vs Clinical Research Associate?

AspectContract Research OrganizationClinical Research Associate
RoleProvides outsourced research services to sponsors, managing entire clinical trials or specific phasesMonitors clinical trials at sites to ensure compliance and data integrity
CredentialsCompany-based, often requires industry experience and certifications in clinical researchTypically requires a degree in life sciences and certifications like CCRP or RAC
Work EnvironmentCorporate setting, project management, client interactionsSite visits, monitoring activities, collaboration with trial sites
Industry UsageUsed by pharmaceutical, biotech, and CRO companiesEmployed by CROs, pharmaceutical companies, and research institutions

In summary, a Contract Research Organization (CRO) manages entire clinical trials for sponsors, while a Clinical Research Associate (CRA) focuses on monitoring and ensuring trial compliance at research sites. Both roles are essential in the clinical research process but differ in scope and responsibilities.

What is a Contract Research Organization (CRO)?

A Contract Research Organization (CRO) is a company that provides support to the pharmaceutical, biotechnology, and medical device industries by offering research services on a contract basis. CROs help clients with various aspects of clinical trials, such as planning, coordinating, monitoring, and managing the trials. They play a crucial role in helping organizations bring new drugs and devices to market efficiently and in compliance with regulatory requirements. By partnering with CROs, companies can access specialized expertise, reduce costs, and accelerate the development process.
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Contract Research Organization jobs near you
Infographic showing various Contract Research Organization job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $149,808 per year, or $72 per hour.

Scientific Account Management Liaison b

RPM ReSearch

On-site

$7M/yr

Full-time

Posted 21 days ago

Job description

Title: Scientific Account Management Liaison- Cell and Gene Therapy

Location: Western Boston

Compensation: 70,000 + 20% bonus/commission

Zero Travel Required- In office position

Services Sold:

Cell and Gene Therapy Analytical Services both GLP and GMP

Potency Release Assays

GMP Lot Release Testing

Vector Infectivity/ Transduction

Neutralizing Antibody Assays

Our client is a preclinical contract research organization that assists pharmaceutical and biopharmaceutical companies in identifying and overcoming research barriers in the development of cell and gene therapies. The client goes deep into each of those areas, offering in-Vivo, in-Situ, and in-Vitro models to assess the properties in question. The company's mission is to continually develop innovative research tools that can be used to accurately predict human outcomes or to explain unanticipated human outcomes when they occur.


Alongside of their enthusiasm for science and research, they have a passion to see each and every one of their employees grow and succeed both personally and professionally. They encourage their employees to continually enhance their ability to contribute to the success of the organization and advance their careers. They are committed to creating an environment where individuals are encouraged to grow and work in collaboration with each other while being passionate about innovation. Their professional culture is a goal-oriented environment full of internally driven and motivated professionals. The company is unique in the fact that there is freedom for autonomy to execute and the ability for each employee to grow in directions that align their individual aspirations with company growth.


Account Manager/ Scientific Account Management Liaison

Account Managers (AMs) are in-house key members of the Sales and Operations Team and function as liaisons between sponsors, internal research scientists, and outside business development team members. AMs use their knowledge of preclinical drug/device testing to design and manage studies for a wide range of sponsor requests ranging from lead optimization through regulatory submissions

Primary responsibilities:

  • Designing studies that meet sponsors’ needs in a scientifically sound and cost-effective manner
  • Providing price quotes for custom projects
  • Providing scientific consultative support for cell and gene therapy analytical services and custom method development.
  • Fostering account diversification and expansion in association with sales and marketing
  • Remaining current on global regulatory requirements and industry trends related to drug and device development

Other important functions include:

  • Managing client expectations with timely and relevant communications
  • Participating in project management
  • Coordinating internal research projects to optimize service offerings
  • Interacting with different teams on a daily basis including scientists, upper management, vendors, legal, and accounting
  • Maintaining accurate records in multiple internal databases

Candidate Requirements:

  • Scientific background is a must. Working knowledge of Cell and Gene Therapy operations and custom PCR or qPCR and/or bioanalysis is highly desirable.
  • Bachelor’s Degree in biology, life sciences, pharmacology, or chemistry. Master’s Degree preferred.
  • 3-5 years relevant industry experience, ideally in a contract research setting, depending on education level
  • - We can also look at individuals from an academic lab looking to get into a more business-oriented position
  • Prior experience in contract research is highly desirable
  • Self-motivated individual with the ability to perform tasks independently with minimal supervision
  • Position requires strong professional communication skills and attention to detail
  • Strong work ethic, self-motivation, and ability to adapt in a dynamic team environment are keys for success