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Clinical Research Associate Cro Jobs in Delaware

CEDENT

Study Start-Up Manager

Wilmington, DE

Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones. * Participate in Local Study Team meetings and report on site performance metrics. * Ensure ...

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Clinical Research Associate Cro information

What is the difference between Clinical Research Associate Cro vs Clinical Trial Assistant?

AspectClinical Research Associate CroClinical Trial Assistant
CredentialsBachelor's degree, often with certifications like CCRP or RACTypically a high school diploma or associate degree, with some roles requiring a certificate
Work EnvironmentConducts site visits, monitors trials, and ensures complianceSupports trial coordination, manages documentation, and assists with logistics
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, CROs, clinical trial teams

The Clinical Research Associate Cro focuses on monitoring clinical trials, ensuring compliance, and site management. In contrast, the Clinical Trial Assistant provides administrative support, manages documentation, and assists with trial logistics. Both roles are essential in clinical research but differ in responsibilities and required experience.

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Clinical Research Associate Cro jobs near you

Research Associate - Analytical Testing

Kelly Services

Newark, DE

$35 - $50/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 2 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

QualificationsEducation

  • 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.