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Full Time Gcp Laboratories Jobs (NOW HIRING)

... 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.

Research Assistant I

Hollywood, FL · On-site

$17.50 - $24.25/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.

Research Assistant

Marlton, NJ · On-site

$19 - $24/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.

Research Assistant I

Hollywood, FL · On-site

$17.50 - $24.25/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.

... full-time employee with a comprehensive benefits package. This role will support the execution of ... Ensure compliance with study protocols, Good Clinical Practice (GCP), institutional policies, and ...

... full-time employee with a comprehensive benefits package. This role will support the execution of ... Ensure compliance with study protocols, Good Clinical Practice (GCP), institutional policies, and ...

Quality Assurance Manager

Redmond, WA · On-site

$120K - $160K/yr

This position is full-time onsite in Redmond, WA and will transition to our new Bothell, WA ... Lead FDA inspection readiness and audits for bioanalytical laboratories, including preparation ...

Showing results 41-60

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.
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:
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 Assistant

CenExel

Englewood, CO • On-site

$19 - $22/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 26 days ago


CenExel rating

7.5

Company rating: 7.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

65th of 120 rated laboratories


Job description

About Us:
CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Job Summary:
With moderate oversight, the Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Compensation: $19-22/h depending on education, experience, and skillset.
Essential Responsibilities and Duties:
  • Creating and maintaining patient charts for all assigned studies.
  • Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
  • Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
  • Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
  • Conducts assessments, including but not limited to, blood pressure, urine collection.
  • Communicating with study participants, caregivers, third party vendors and laboratories as needed.
  • Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
  • Aiding Coordinators in the facilitation of study monitoring visits.
  • Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:
  • High school graduate or equivalent.
  • Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
  • Skilled in organization and record maintenance.
  • Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
  • Strong personal initiative and attention to detail.
  • Ability to react calmly and effectively in emergency situations.
  • Ability to interpret, adapt and apply guidelines and procedures.
  • Ability to clearly communicate both orally and verbally.

Working Conditions
  1. Indoor, Office environment.
  2. Essential physical requirements include sitting, typing, standing, and walking.
  3. Lightly active position, occasional lifting of up to 20 pounds and/or pushing carts up to 50 pounds
  4. Reporting to work, as scheduled, is essential.
  5. On site work arrangement.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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