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Clinical Trials Project Manager

labcorp

Full-time
USA
$65k-$85k per year
project management
qa
leadership
documentation
communication
The job listing has expired. Unfortunately, the hiring company is no longer accepting new applications.

To see similar active jobs please follow this link: Remote Management jobs

Labcorp is seeking a remote Clinical Trials Project Manager to join our team!

Work Schedule

Monday - Friday, Day Shift

Job Responsibilities

  • Ensure successful delivery of assigned clinical trial projects by aligning study specifications and deliverables with client, protocol, and internal requirements.

  • Clearly document and manage project scope, timelines, and expectations.

  • Coordinate cross‑functional activities including logistics, specimen management, data management, and laboratory operations.

  • Direct timelines and resource needs with relevant internal departments.

  • Ensure all validation and quality control requirements are met and documented according to SOPs and obtain all necessary internal and client approvals.

  • Organize and lead client meetings and training sessions; maintain complete documentation of all training.

  • Provide day‑to‑day project management through internal and external coordination throughout the project lifecycle.

  • Troubleshoot issues related to specimens, result reporting, and site compliance; provide timely resolutions or escalation as needed.

  • Monitor project progress through regular team meetings and provide updates and metrics to management.

  • Proactively identify project risks and escalate issues following global escalation policies.

  • Maintain consistent, clear communication with clients and internal leadership on project status.

  • Manage manual invoicing processes to ensure accuracy and alignment.

  • Collaborate with Quality Assurance during audits, inspections, and other QA/QC activities; respond promptly to information requests.

  • Complete all tasks in compliance with SOPs and policies and maintain required training documentation.

  • Support process improvement initiatives, standardization efforts, and SOP development or review.

  • Perform additional duties as assigned by management.

Minimum Qualifications

  • Bachelor’s Degree in science, laboratory, or health related disciplines

  • 2 years or more of clinical trials experience

  • 2 years or more working within Microsoft Office applications

Preferred Qualifications

  • 5 years or more years’ experience in a clinical trials environment

  • 1 year or more years’ experience working in LCLS, Salesforce, Periscope and Link 

Additional Job Standards

  • This position requires excellent written and verbal communication skills, strong organization skills and mindfulness, time management and prioritization skills, negotiation skills, presentation skills, and the ability to work in a fast-paced team environment.

About Labcorp

At Labcorp, we are a global leader of innovative and comprehensive laboratory services that helps doctors, hospitals, pharmaceutical companies, researchers and patients make clear and confident decisions.

Through our unparalleled diagnostics and drug development laboratory capabilities, our nearly 70,000 employees combine cutting-edge innovation, science and technology to solve some of today’s biggest health challenges, accelerate life-changing healthcare breakthroughs and impact lives around the world.

Here, you are empowered to own your career journey and create a personalized development plan with the support of your team.

Application Window: March 10, 2026 - March 13, 2026

Pay Range: $65,000 - $85,000

All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. 

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. 

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

About the job

Full-time
USA
Mid Level
$65k-$85k per year
Posted 2 days ago
project management
qa
leadership
documentation
communication
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Clinical Trials Project Manager

labcorp
The job listing has expired. Unfortunately, the hiring company is no longer accepting new applications.

To see similar active jobs please follow this link: Remote Management jobs

Labcorp is seeking a remote Clinical Trials Project Manager to join our team!

Work Schedule

Monday - Friday, Day Shift

Job Responsibilities

  • Ensure successful delivery of assigned clinical trial projects by aligning study specifications and deliverables with client, protocol, and internal requirements.

  • Clearly document and manage project scope, timelines, and expectations.

  • Coordinate cross‑functional activities including logistics, specimen management, data management, and laboratory operations.

  • Direct timelines and resource needs with relevant internal departments.

  • Ensure all validation and quality control requirements are met and documented according to SOPs and obtain all necessary internal and client approvals.

  • Organize and lead client meetings and training sessions; maintain complete documentation of all training.

  • Provide day‑to‑day project management through internal and external coordination throughout the project lifecycle.

  • Troubleshoot issues related to specimens, result reporting, and site compliance; provide timely resolutions or escalation as needed.

  • Monitor project progress through regular team meetings and provide updates and metrics to management.

  • Proactively identify project risks and escalate issues following global escalation policies.

  • Maintain consistent, clear communication with clients and internal leadership on project status.

  • Manage manual invoicing processes to ensure accuracy and alignment.

  • Collaborate with Quality Assurance during audits, inspections, and other QA/QC activities; respond promptly to information requests.

  • Complete all tasks in compliance with SOPs and policies and maintain required training documentation.

  • Support process improvement initiatives, standardization efforts, and SOP development or review.

  • Perform additional duties as assigned by management.

Minimum Qualifications

  • Bachelor’s Degree in science, laboratory, or health related disciplines

  • 2 years or more of clinical trials experience

  • 2 years or more working within Microsoft Office applications

Preferred Qualifications

  • 5 years or more years’ experience in a clinical trials environment

  • 1 year or more years’ experience working in LCLS, Salesforce, Periscope and Link 

Additional Job Standards

  • This position requires excellent written and verbal communication skills, strong organization skills and mindfulness, time management and prioritization skills, negotiation skills, presentation skills, and the ability to work in a fast-paced team environment.

About Labcorp

At Labcorp, we are a global leader of innovative and comprehensive laboratory services that helps doctors, hospitals, pharmaceutical companies, researchers and patients make clear and confident decisions.

Through our unparalleled diagnostics and drug development laboratory capabilities, our nearly 70,000 employees combine cutting-edge innovation, science and technology to solve some of today’s biggest health challenges, accelerate life-changing healthcare breakthroughs and impact lives around the world.

Here, you are empowered to own your career journey and create a personalized development plan with the support of your team.

Application Window: March 10, 2026 - March 13, 2026

Pay Range: $65,000 - $85,000

All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. 

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. 

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

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