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Gcp Laboratories Jobs (NOW HIRING)

Clinical Research Coordinator 2

Seattle, WA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

Occasional travel to partner laboratories or study sites may be required (estimated up to 10%) * GCP and IATA training (to be completed within 30 days of hire if not already held) * Able to lift and ...

Clinical Research Coordinator 2

Seattle, WA · On-site

$75K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Occasional travel to partner laboratories or study sites may be required (estimated up to 10%) * GCP and IATA training (to be completed within 30 days of hire if not already held) * Able to lift and ...

Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to ... Maintain knowledge of Good Clinical Practices (GCP), Standard Operating Procedures (SOP), and ...

Oncology Infusion Nurse (RN)

Los Angeles, CA · On-site

$43.27 - $57.69/hr

Adhere to Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements ... environments (laboratories, clinical settings), handling hazards chemicals or lab specimens ...

Biospecimen Operations Manager

Wilmington, DE

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Participate in program meetings with central laboratories, clinical teams, operations, and data ... GCP). * Advanced skills in Microsoft Office applications. * Good working knowledge of electronic ...

Associate Research Scientist

Gaithersburg, MD · On-site

$75K - $100K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Our expert scientists perform large molecule bioanalysis, assay development, validation, and sample analysis at our GLP, GCP, and CLIA compliant laboratories. Smithers is seeking a talented Associate ...

... GCP) guidelines. This is an ideal opportunity for recent graduates, Medical Assistants, or aspiring ... environments (laboratories, clinical settings), handling hazards chemicals or lab specimens ...

Lab Supervisor

Columbus, OH · On-site

  • Medical

  • Dental

  • Retirement

  • PTO

Ensure compliance with CLIA, GLP, GCP, IRB requirements, SOPs, OSHA standards, and applicable ... laboratories when appropriate. * Serve as a backup point of contact for sponsors and internal ...

Cloud Security Architect

Westbrook, ME · On-site

$66.50 - $88.50/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

IDEXX is seeking a Cloud Security Architect to lead our multi-cloud security architecture across AWS, Azure, and GCP environments. This senior-level position will architect and implement cloud ...

Lab Technician

Philadelphia, PA

$19.25 - $25.50/hr

Prepares, processes, and ships laboratory samples to outside laboratories following IATA ... ICH/GCP and Optimal Research Standing Operating Procedures. * Knowledgeable of the Sponsor ...

Lab Technician

Philadelphia, PA · On-site

$19.25 - $25.50/hr

Prepares, processes, and ships laboratory samples to outside laboratories following IATA ... ICH/GCP and Optimal Research Standing Operating Procedures. * Knowledgeable of the Sponsor ...

Showing results 41-60

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 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.

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 cities are hiring for Gcp Laboratories jobs?

Cities with the most 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 Gcp Laboratories jobs?

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

Infographic showing various Gcp Laboratories job openings in the United States as of August 2026, with employment types broken down into 2% Internship, 1% As Needed, 90% Full Time, 6% Part Time, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Clinical Research Coordinator 2

Tasso

Seattle, WA • On-site

Full-time

Medical, Dental, Vision, Retirement

Posted 14 days ago


Job description

Who We Are 

Tasso is a fast-growing Seattle-based startup focused on delivering at-home diagnostic testing to those who need it most. We are growing our footprint with leading health systems, clinical research organizations, academic medical centers, and more who are looking to deliver clinical-grade, convenient diagnostic tests to their patients. Tasso was originally founded to find a better way to collect blood instead of a painful fingerstick or time-consuming venous draw. Since then, our products have been used in pharmaceutical clinical trials, by Olympians as part of a new virtual anti-doping program, and broadly by hospital systems across the US. 

We are looking for a Clinical Research Coordinator 2, a Seattle-based role responsible for handling clinical research study materials and specimens for the Clinical team. This position will report to our Associate Director, Clinical Operations. An ideal candidate will have at a minimum 2 years’ experience in a participant-facing clinical research setting.
 

What You Will Do 
Conduct Clinical Research Studies:

  • Recruit, prescreen, and obtain informed consent from prospective study participants
  • Conduct clinical study visits, including collecting medical history, performing protocol-specified procedures and phlebotomy, and recording source data
  • Provide study devices to participants and educate them on proper use
  • Collect, process, and prepare specimens in accordance with clinical and laboratory protocols
  • Maintain screening logs, enrollment logs, and participant records, both manually and electronically
  • Enter and validate study data, e.g., into electronic data capture (EDC) platforms or study spreadsheets
  • Support protocol compliance and participate in quality reviews of study activities
  • Travel to partner laboratories, at-home collection sites, and additional clinic locations to support enrollment and data collection
Provide data and documentation support:
  • Support clinical and laboratory data cleaning, reconciliation, and query resolution across active studies, in partnership with the study team
  • Assist with data listings, discrepancy review, and routine EDC data management tasks
  • Maintain regulatory and essential documents and support Study Master File (SMF) upkeep
  • Assist with study start-up and close-out activities and associated documentation

Who You Are 

  • Authorized to work in the United States
  • Primarily on-site in Seattle five days per week - candidates outside of the Seattle area will not be considered for this role
  • Bachelor’s Degree in a biological or health science field
  • At least two years of experience in a clinical research coordinator or comparable role
  • Medical Assistant Phlebotomist certification for Washington State, or readiness to obtain it
  • Working knowledge of medical terminology, clinical trials, and Good Clinical Practice (GCP)
  • Comfort working with clinical/laboratory data and research data systems; experience with EDC platforms preferred
  • Proficiency with Microsoft Office and willingness to learn other research systems, e.g., EDC.
  • Strong attention to detail, organizational skills, and the ability to manage multiple tasks across concurrent programs
  • Ability to work both independently and as part of a distributed team
  • Phlebotomy certification preferred (to be completed within 30 days of hire if not already held)
  • Proficiency with Microsoft Office and willingness to learn research inventory and data systems
  • Occasional travel to partner laboratories or study sites may be required (estimated up to 10%)
  • GCP and IATA training (to be completed within 30 days of hire if not already held)
  • Able to lift and handle laboratory shipments and supplies as needed
  • Able to perform other responsibilities as assigned

What We Offer 

$75K/yr - $90K/yr base salary + Stock Options 

We offer competitive compensation, benefits and a fantastic work environment: 

  • 95% paid Medical, 100% Dental & Vision for employees and a generous subsidy for dependents 

  • 11 Paid Holidays and generous Time Off policies 

  • 401K + Employer Match 

  • Paid parental leave policy 

We have a strong healthcare-driven mission, and your guidance and efforts will directly link to our success.  We embrace diversity and equal opportunity and are committed to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be for it. 

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