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Contract Research Associate information

What are the key skills and qualifications needed to thrive as a contract research associate?

To thrive as a Contract Research Associate, you need a solid background in life sciences or a related field, attention to detail, and experience with clinical research processes. Familiarity with regulatory systems like FDA guidelines, Good Clinical Practice (GCP), data management tools, and electronic data capture (EDC) systems is typically required. Strong organizational skills, effective communication, and the ability to work independently or in teams help set candidates apart. These competencies ensure that clinical trials are conducted accurately, compliantly, and efficiently, supporting successful research outcomes.

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

AspectContract Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP beneficialBachelor's degree in health sciences or related field; certifications like CCRP or CCRC advantageous
Work EnvironmentTypically in pharmaceutical or biotech companies, contract research organizations (CROs)Usually in hospitals, clinics, or research sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, academic medical centers, research institutions
Common Search & ComparisonYesYes

While both roles support clinical trials, a Contract Research Associate primarily works for pharmaceutical or biotech companies managing trial processes remotely or at sites, often on a contractual basis. A Clinical Research Coordinator typically works directly at research sites, coordinating patient visits and data collection. Both roles require similar credentials and certifications, but their work environments and employer types differ.

What are some typical challenges faced by contract research associates when managing multiple studies simultaneously?

Contract Research Associates often juggle several clinical trials at once, which can pose challenges in time management and prioritization. Balancing the requirements of different sponsors, adhering to varying protocols, and ensuring accurate documentation for each study demand strong organizational skills. Additionally, staying up to date with regulatory changes and effective communication with site staff are crucial to avoid delays and ensure compliance. Developing efficient workflows and leveraging project management tools can help address these challenges.

What is a contract research associate?

A Contract Research Associate (CRA) is a professional who is typically hired on a contractual basis to support and manage clinical trials or research projects. Their primary responsibilities include monitoring research sites, ensuring compliance with protocols and regulations, collecting and verifying data, and maintaining proper documentation. CRAs play a critical role in ensuring the integrity and safety of clinical studies, often working for pharmaceutical companies, contract research organizations (CROs), or academic institutions. The contract nature of the role means that assignments are usually project-based and may vary in duration and scope.
What cities in Delaware are hiring for Contract Research Associate jobs? Cities in Delaware with the most Contract Research Associate job openings:
Contract Research Associate jobs near you

Research Associate - Analytical Testing

Kelly Services

Newark, DE • On-site

$35 - $50/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 29 days ago

Job description

Kelly Science & Clinical is hiring a Research Associate for a full-time contract opportunity in Newark, DE.

About the Role

In this laboratory-based role, you will support analytical testing for toxicity studies involving agricultural products, intermediates, metabolites, and impurities. Working under the guidance of a Principal Investigator, you will apply modern chromatographic and mass spectrometry techniques to generate high-quality analytical data in a GLP-regulated environment.

This opportunity is ideal for an analytical chemist with experience in chromatography, method development, and regulated laboratory environments who enjoys solving complex analytical challenges while supporting toxicology and regulatory studies.

What You'll Do

  • Perform routine and non-routine analysis of toxicity study samples, including dose and diet formulations, in vitro samples, and animal matrices

  • Prepare, extract, and purify samples for chromatographic and mass spectrometric analysis

  • Develop and optimize chromatographic methods to separate, identify, and quantify active compounds and metabolites

  • Operate, calibrate, maintain, and troubleshoot analytical instrumentation including HPLC, UHPLC, LC/UV, LC-MS/MS, radiochemical detectors, liquid scintillation counters, and fraction collectors

  • Generate accurate, reliable, and reproducible analytical data to support GLP studies and technical reports

  • Perform laboratory work in compliance with Good Laboratory Practice (GLP) and other applicable regulatory guidelines

  • Maintain detailed laboratory documentation and ensure data integrity

  • Perform routine laboratory and analytical equipment maintenance

  • Collaborate with scientists and project teams to meet study timelines and project objectives

Qualifications Education

  • Bachelor's degree in Chemistry or a related scientific discipline required

  • Master's degree is welcome

  • Ph.D. candidates are not the target profile for this opportunity

Experience

  • Minimum of 5 years of experience in a GLP laboratory environment

  • Hands-on experience with HPLC, UHPLC, and chromatographic method development

  • Experience with LC/MS and LC-MS/MS analytical techniques

  • Experience handling radiolabeled (¹?C) samples is highly preferred

  • Experience supporting regulated analytical testing and GLP documentation

Key Skills

  • Strong analytical chemistry and chromatography expertise

  • Experience developing and optimizing analytical methods

  • Excellent troubleshooting and problem-solving skills

  • Strong attention to detail and organizational abilities

  • Ability to manage multiple projects while meeting deadlines

  • Effective written and verbal communication skills

  • Ability to work independently and collaboratively in a laboratory environment

  • Familiarity with chromatography data systems and analytical instrument software

Preferred Background

  • Experience supporting toxicology, agrochemical, environmental, pharmaceutical, or regulatory studies

  • Experience with radiochemical analytical techniques and ¹?C sample handling

  • Knowledge of biological sample extraction and purification

  • Familiarity with GLP regulations and regulated laboratory documentation

Additional Details

  • Location: Newark, DE

  • Job Type: Full-time Contract

  • Schedule: Monday–Friday, 8:00 AM–5:00 PM

  • Pay Rate: $35–50/hour, depending on experience

Take the next step in your analytical chemistry career with Kelly Science & Clinical—apply today to join a collaborative team supporting innovative toxicology and analytical research.


As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.

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