ZipRecruiter

Log In

1

Preclinical Research Associate Jobs in Delaware (NOW HIRING)

Charles River

Molecular Technologist I

Newark, DE · On-site

$22/hr

  • Medical

  • Retirement

  • PTO

S.) or Associates Degree in Biology or related discipline required. * 0-2 years of experience in ... About Charles River Charles River is an early-stage contract research organization (CRO). We have ...

All JobsPreclinical Research Associate JobsPreclinical Research Associate Jobs in Delaware

Preclinical Research Associate information

What is a preclinical research associate?

Preclinical Research Associates are professionals who support scientific studies that evaluate the safety and efficacy of new drugs, medical devices, or treatments before they are tested in humans. They are responsible for conducting laboratory experiments, collecting and analyzing data, and ensuring compliance with regulatory standards. Their work is crucial for identifying potential risks and optimizing study protocols, laying the groundwork for clinical trials. Preclinical Research Associates typically work in pharmaceutical companies, biotechnology firms, or academic research settings, collaborating closely with scientists and regulatory teams.

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

A Preclinical Research Associate needs a solid background in life sciences, laboratory techniques, and data analysis, typically supported by a bachelor's degree in biology, pharmacology, or a related field. Familiarity with laboratory information management systems (LIMS), animal handling protocols, and regulatory standards such as GLP is often required. Strong attention to detail, problem-solving abilities, and effective teamwork are valuable soft skills in this role. These competencies are essential to ensure accurate experimental results, compliance with research regulations, and effective collaboration within research teams.

What are some common challenges faced by preclinical research associates and how can they be managed?

Preclinical Research Associates often encounter challenges such as managing tight project timelines, adapting to evolving experimental protocols, and ensuring strict adherence to regulatory guidelines. Balancing multiple studies simultaneously can require strong organizational and communication skills, especially when collaborating with cross-functional teams like scientists, veterinarians, and data analysts. Staying proactive in seeking feedback, participating in regular team meetings, and consistently documenting experimental procedures help manage these challenges and ensure high-quality results.

What is the difference between Preclinical Research Associate vs Laboratory Technician?

AspectPreclinical Research AssociateLaboratory Technician
Required CredentialsBachelor's degree in life sciences; some roles may require experience in researchAssociate's degree or relevant certification; entry-level
Work EnvironmentResearch labs in biotech/pharmaceutical companies; clinical trial settingsLaboratories performing routine tests and experiments
Employer & Industry UsageUsed in biotech, pharma, and research institutions for drug developmentCommon in clinical labs, hospitals, and research facilities
Comparison Search IntentUnderstanding research roles in drug developmentLearning about lab support roles in scientific settings

The Preclinical Research Associate and Laboratory Technician roles both work within laboratory environments, but the associate typically engages in more complex research activities related to drug development, requiring a higher level of education and specialized knowledge. The technician role focuses on routine lab tasks and support functions. Both positions are essential in scientific research, but they differ in responsibilities and career progression.

What are popular job titles related to Preclinical Research Associate jobs in Delaware?

For Preclinical Research Associate jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Preclinical Research Associate jobs in Delaware look for?

The top searched job categories for Preclinical Research Associate jobs in Delaware are:

What cities in Delaware are hiring for Preclinical Research Associate jobs?

Cities in Delaware with the most Preclinical Research Associate job openings:

Preclinical Research Associate jobs near you
Infographic showing various Preclinical Research Associate job openings in Delaware as of August 2026, with employment types broken down into 88% Full Time, and 12% Contract. Highlights an 92% In-person, and 8% Hybrid job distribution.

Associate Scientist I - Bioanalytical Dept

QPS, LLC

Newark, DE • On-site

$45K - $50K/yr

Full-time

Life, Retirement

Re-posted 11 days ago

Job description

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS, LLC has an opening for an Associate Scientist I in our Bioanalytical department. In this role, you will play a pivotal part in QPS’ continued expansion of our bioanalytical capabilities to support small molecule, antibody drug conjugate, protein, and gene therapy drug development. The LC-MS group’s expertise lies in the quantitation of small molecules, oligonucleotides, peptides, proteins, and metabolite biomarkers by various mass spectrometric (LC-MS/MS, LC‑HRMS, hybrid/immunoaffinity mass spec), and hybridization-LC-fluorescence techniques.


As an Associate Scientist I, you will be a fully-supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations.


No visa sponsorship (e.g. H‑1B, L‑1, E) will be provided for this active position, now or in the future. Applicants must currently be authorized to work in the U.S. on a permanent or unrestricted basis.


QPS’ Story:

Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.


Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.


If this sounds like your ideal work environment, then we would love to speak with you, so apply today!


Please visit our website (www.qps.com) for more information and to see all current openings.


The Job

  • Perform routine lab operations, such as sample extraction, preparing reagents, operating automatic liquid handling equipment, pipetting, weighing, monitoring, and recording, in a neat/clean manner
  • Assist Principal Investigator in performing quantitative analysis of drug and metabolites in biological samples utilizing validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods under GLP regulations
  • Document experiment details, calculations, results and observations in accordance with GLPs and SOPs
  • Basic math skills to perform routine calculations


Work Location

  • This job will be 100% QPS-office/facility based


Requirements

The successful candidate will hold a degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline as follows:

  • Bachelor’s degree


Why You Should Apply

  • Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.
  • Structured Career Ladders that provide excellent growth based on your personal aspirations.
  • Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.
  • Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance
  • Park-like setting in Newark, Delaware
  • Internal committees designed with the needs and enjoyment of QPS employees in mind.


QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.