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Full Time Gcp Laboratories Jobs (NOW HIRING)

Medix

Research Assistant (RA)

Walnut Creek, CA · On-site

$20 - $22/hr

... GCP) guidelines. This is an ideal opportunity for recent graduates, Medical Assistants, or aspiring ... Ability to work on-site Monday through Friday (Full-Time) within one of the following shifts based ...

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Full Time Gcp Laboratories information

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.

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 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 cities are hiring for Full Time Gcp Laboratories jobs?

Cities with the most Full Time Gcp Laboratories job openings:

What are the most commonly searched types of Gcp Laboratories jobs?

The most popular types of Gcp Laboratories jobs are:

What states have the most Full Time Gcp Laboratories jobs?

States with the most job openings for Full Time Gcp Laboratories jobs include:

What job categories do people searching Full Time Gcp Laboratories jobs look for?

The top searched job categories for Full Time Gcp Laboratories jobs are:

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 93% Full Time, 1% Part Time, and 6% Contract. Highlights an 75% Physical, 7% Hybrid, and 18% Remote job distribution.

Data Management Specialist

Frontage Laboratories

Exton, PA • On-site

Full-time

Medical, Dental, Life, Retirement

Re-posted 9 days ago

Job description

Data Management Specialist

JOB TITLE: Data Management Specialist


DEPARTMENT: Central Lab Services – IT

Full-time

Exton, PA

PURPOSE: Manage data transfers between Frontage and clients and internal reporting from data systems, per company SOPs and relevant regulations and requirements.

Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Roles and Responsibilities:

  • Participate in project meetings to understand study protocol and capture clinical trial data elements that we need to capture in our system, particularly those that will need to be reported internally and transferred to our clients.
  • Work with LIS Application Specialist to make sure those data elements are setup correctly in the system.
  • Work with Project Managers and clients to create Data Transfer Agreement (DTA).
  • Build and maintain data management templates for internal reporting and external transfer.
  • Create process to generate project-specific export of data from or import data to LIS/LIMS and other systems.
  • Work with Quality Assurance to make sure data accuracy in reports and data transfer.
  • Ensure the data transfers are carried out according to the corresponding agreements in a timely manner.
  • Assist with development of departmental data management procedures and ensure compliance with relevant regulations and requirements (HIPAA, GDPR, GCP, GLP, CAP, CLIA, etc.) in conjunction with QA and laboratory management.
  • Other tasks as assigned.


Qualifications and Skills:

  • Bachelor’s degree in the STEM field or equivalent work experience.
  • At least one year of clinical data management or equivalent work experience.
  • Good skills with office software such as Word, Excel Formula & Power Query, etc.
  • Knowledge or experience of SQL is a great plus.

Salary and Benefits:

Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance.

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.