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Full Time Gcp Laboratories Jobs (NOW HIRING)

Rochester Regional Health

$70K - $80K/yr

... Laboratories. The Research & Development Specialist will develop comprehensive policies and ... Participation in all activities that seek to ensure compliance with GCP guidelines and ...

PICTOR LABS INC

$89K - $123K/yr

... laboratories to advance their digital pathology capabilities while reducing chemical waste ... Pictor Labs Employment Type: Full-time Responsibilities * Design, development, and optimization of ...

Round Rock High School

$70K - $80K/yr

... Laboratories. The Research & Development Specialist will develop comprehensive policies and ... Participation in all activities that seek to ensure compliance with GCP guidelines and ...

NVA

Veterinary Internal Medicine Specialist

Orland Park, IL · On-site

$200K - $250K/yr

Premier Veterinary Group, located in in Orland Park, Illinois, is looking for a full-time Internal ... From sampling requests to GCP studies, there is something for everyone, and we make it easy for you ...

CenExel

Medical Assistant - Clinical Research

Anaheim, CA · On-site

$20 - $21/hr

... full-time employees after 30 days of employment, including Health Insurance, Dental, Vision, LTD ... Communicating with study participants, caregivers, third party vendors and laboratories as needed.

CenExel

Medical Assistant - Clinical Research

Torrance, CA · On-site

$20 - $22.50/hr

... Full-Time Monday - Friday (8:00 am - 04:30 pm) Job Summary: Provides direct support to Clinical ... Communicating with study participants, caregivers, third party vendors and laboratories as needed.

New

CenExel

Research Assistant

Decatur, GA · On-site

$20 - $21/hr

... full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD ... Communicating with study participants, caregivers, third party vendors and laboratories as needed.

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Full Time Gcp Laboratories information

What is the difference between Full Time Gcp Laboratories vs Full Time Gcp Laboratories?

AspectFull Time Gcp LaboratoriesFull Time Gcp Laboratories
CredentialsTypically requires GCP certifications, laboratory safety training, and relevant science degreesSame as above
Work EnvironmentLaboratory settings with hands-on testing, experiments, and data analysisSame as above
Industry UsageCommonly employed in biotech, pharmaceuticals, and research institutionsSame as above
Job FocusConducting experiments, managing lab equipment, ensuring safety protocolsSame as above

Both roles of Full Time Gcp Laboratories involve working in laboratory environments with similar credentials, industry applications, and job responsibilities. The key differences are minimal, often related to specific employer requirements or project focus.

What are some common challenges faced by professionals working full time in GCP laboratories, and how can they be managed?

Professionals in full-time GCP laboratories often face challenges such as maintaining strict adherence to regulatory standards, managing large volumes of documentation, and coordinating effectively with multidisciplinary teams. Staying updated with the latest compliance protocols and ensuring accurate data entry are critical for success. Proactively communicating with colleagues and participating in ongoing training can help manage these responsibilities efficiently, ensuring high-quality and reliable laboratory outcomes.

What is a full time GCP laboratory?

Full Time GCP Laboratories refer to laboratory facilities that operate under Good Clinical Practice (GCP) guidelines on a full-time basis, supporting clinical research and trials. These labs ensure that data collected during clinical studies is accurate, reliable, and meets regulatory standards. They are staffed by trained professionals and equipped to handle a variety of tests and analyses required during clinical development. Working full-time in a GCP laboratory typically means being involved in all stages of clinical research, including sample handling, data management, and quality control.

What are the key skills and qualifications needed to thrive as a GCP laboratory professional?

To thrive as a GCP Laboratory Professional, you need a solid background in laboratory sciences, regulatory compliance, and Good Clinical Practice (GCP) guidelines, typically supported by a relevant degree in science or laboratory technology. Familiarity with laboratory information management systems (LIMS), quality assurance software, and certification in GCP or related regulatory frameworks is often required. Attention to detail, strong organizational skills, and effective communication are vital soft skills for ensuring accurate data and smooth collaboration. These competencies are essential to maintain the integrity of clinical trial data and ensure compliance with strict regulatory standards.
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Full Time Gcp Laboratories jobs near you
Infographic showing various Full Time Gcp Laboratories job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Clinical Research Coordinator

Eurofins Scientific

Piscataway, NJ • On-site

$20/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 25 days ago

Eurofins rating

7.4

Company rating: 7.4 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

69th of 120 rated laboratories

Job description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

Pay Range: $20.00/Hr.

Shift: Monday- Friday, 9:30am- 6:00pm

Primary Duties and Responsibilities of a CRC

  • Act as project manager on studies as directed by department manager.
  • Assist in the conduct of clinical studies as specified by the study protocol under the supervision of designated Principal Investigator and departmental management.
  • Record observations, measurements, and test results, as required.
  • Provide a professional experience to test subjects, and answer all inquiries, as appropriate
  • Assist in the preparation of test materials, as needed.
  • Perform data entry and data review to ensure study quality.
  • Conduct studies in accordance to ECRL Standard Operating Procedures study protocol and ICH GCP.
  • Efficiently time manage multiple projects.
  •  Succinctly communicate day to day project details to both department manager and Principal Investigator.
  • Perform department specific procedures as qualified by training and evaluation of proficiency (clinical study evaluations and measurements)
  • Process study data and prepare for reporting and conclusions.
  • Maintain awareness of all ongoing study activities throughout the day and provide leadership with accurate updates regarding clinic operations.
  • Serve as the primary point of contact for the clinical team during closing shifts, providing real-time updates on subject flow, study progress, and operational issues.
  • Monitor daily clinic workflow and proactively identify and resolve operational bottlenecks.
  • Prepare and communicate a comprehensive end-of-day status report, highlighting completed visits, pending tasks, protocol deviations, adverse events, and issues requiring management follow-up.
Qualifications
  • High School Diploma
Additional Information

Pay Range: $20.00/Hr.

Shift: Monday- Friday, 9:30am- 6:00pm

What we offer:

  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

Eurofins USA Consumer Product Testing is a Disabled and Veteran Equal Employment Opportunity employer.

What Eurofins employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US

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