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Gcp Laboratories Jobs (NOW HIRING)

BrainChild Bio

Clinical Research Associate (CRA)

Assess site compliance with GCP, protocol requirements, institutional policies, and regulatory ... local laboratories, and radiology departments, to ensure coordinated execution of protocol ...

CatalYm GmbH

$68.52 - $85.65/hr

Coordinate activities with external vendors, specialty laboratories, central laboratories, CROs ... Good understanding of GCP, clinical trial quality requirements, sample traceability, vendor ...

Systimmune

Associate Director, Clinical QA

Princeton, NJ · On-site

$150K - $190K/yr

Lead quality oversight activities for CROs, pharmacovigilance vendors, laboratories, technology providers, and other GCP/GVP service providers. * Support vendor qualification, risk assessments ...

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Gcp Laboratories information

What is a GCP Laboratories job?

A GCP Laboratories job typically involves conducting clinical trials and laboratory testing in compliance with Good Clinical Practice (GCP) guidelines. Professionals in this role ensure that laboratory procedures adhere to regulatory standards for accuracy, reliability, and ethical conduct. They may work in pharmaceutical companies, research institutions, or healthcare organizations, supporting drug development and medical research. Key responsibilities often include sample analysis, data recording, quality control, and regulatory compliance.

What are the key skills and qualifications needed to thrive in the GCP Laboratories position?

To excel at GCP (Good Clinical Practice) Laboratories, candidates typically need a background in life sciences or laboratory technology, with strong knowledge of clinical trials and regulatory compliance. Familiarity with specialized laboratory equipment, Laboratory Information Management Systems (LIMS), and GCP certification are highly valuable. Attention to detail, analytical thinking, and effective teamwork enable professionals to maintain accuracy and integrity in clinical test results. These skills and qualities are critical for ensuring the reliability of data used in medical research and for meeting regulatory requirements.

What are the typical day-to-day responsibilities for someone working at a GCP Laboratory?

In a GCP Laboratory, your daily tasks often include preparing, analyzing, and documenting clinical samples with strict adherence to regulatory protocols. You’ll work closely with clinical research teams to ensure data accuracy and regulatory compliance, while also maintaining detailed laboratory records and quality control logs. Collaboration is a key part of the role, as you may participate in team meetings, communicate findings, and help implement process improvements. These responsibilities offer a dynamic work environment focused on supporting vital clinical research projects with precision and integrity.

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Gcp Laboratories jobs near you
Infographic showing various 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 77% Physical, 6% Hybrid, and 17% Remote job distribution.

Associate Project Manager I

ARUP Laboratories

Salt Lake City, UT • On-site

$22.12/hr

Full-time

Re-posted 15 days ago

ARUP Laboratories rating

7.3

Company rating: 7.3 out of 10

Based on 40 frontline employees who took The Breakroom Quiz

73rd of 121 rated laboratories

Job description

Schedule:
Monday - Friday (40 hrs/wk)
8:00 AM - 5:00 PM
Department: PharmaDx - 511
Primary Purpose:
The Associate Project Manager I is an entry-level position responsible for providing collaborative support to the groups pharmaceutical projects. An Associate Project Manager I supports the planning, scheduling, monitoring, and controlling aspects of projects and works closely with Project and Program Managers on assigned projects. An Associate Project Manager I may manage small straightforward projects or sub-projects with more autonomy, as assigned.
Position may specialize in functional areas, such as Information Technology or Laboratory, which may require additional specific skill and experience.
About ARUP:
ARUP Laboratories is a national clinical and anatomic pathology reference laboratory and an enterprise of the University of Utah and its Department of Pathology. Based in Salt Lake City, Utah.
ARUP proudly hires top talent to create a work environment of diversity, professional growth and continuous development. Our workforce is committed to the important service we provide to over one million patients each month. We always strive for excellence and have a strong desire to have involvement with the advances in medicine and the role laboratory services plays within each patient's life. We never forget that there is a patient behind every specimen we receive.
We are looking for individuals who want to contribute to ARUP's culture of accountability, integrity, service, and excellence. Consider joining our dynamic team.
Essential Functions:
Supports department staff in project management activities.
Assists in the planning and implementation of projects with oversight.
Supports aspects of complex projects as requested.
Responsible for learning and implementing Good Clinical Practices (GCP) and Medical Device Design Control requirements for projects.
Coordinates and collaborates with subject matter experts to conduct data analysis and risk assessments in relation to compliance with established procedures.
Presents analysis results to managers or senior management.
Coordinates communications as warranted by project scope.
Tracks proposed projects and track and resolve issues related to the proposed projects.
Functions as liaison with internal customers on projects.
Ensures that proper processes are being followed and assist in establishing new processes as required.
Other duties as assigned
Physical and Other Requirements:
Stooping: Bending body downward and forward by bending spine at the waist.
Reaching: Extending hand(s) and arm(s) in any direction.
Mobility: The person in this position needs to occasionally move between work sites and inside the office to access file cabinets, office machinery, etc.
Communicate: Frequently communicate with others.
PPE: Biohazard laboratory environment that requires use of personal protective equipment in accordance with CDC and OSHA regulations and company policies.
ARUP Policies and Procedures: To conduct self in compliance with all ARUP Policies and Procedures.
Sedentary Work: Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects.
Fine Motor Control: Picking, pinching, typing or otherwise working, primarily with fingers rather than with the whole hand as in handling.
Vision: Having close, far, and peripheral visual acuity to perform a variety of tasks such as make general observations of depth and distance.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
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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