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Contract Labcorp Clinical Trials Jobs (NOW HIRING)

Clinical Dynamix

Clinical Trials Manager

Burlington, MA · On-site

Clinical Trials Manager The Clinical Trials Manager is responsible for the delivery of a key phase ... Support study budgets and contracts in collaboration with finance and legal teams. * Contribute to ...

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Stamford Health

Clinical Trials Manager-B

Stamford, CT

  • Medical

  • Retirement

  • PTO

Reviews contract, consent, budget, amendments, and other modifications to documentation for appropriateness. Acts as liaison between SH legal, clinical trials program and CRO/Sponsor to insure ...

Stamford Health

Clinical Trials Manager-B

Stamford, CT · On-site

  • Medical

  • Retirement

  • PTO

Reviews CDA and manages CDA process. • Reviews contract, consent, budget, amendments, and other ... clinical trials program and CRO/Sponsor to insure consistency of documents and compliance with ...

Stamford Health

Clinical Trials Manager-B

Stamford, CT

  • Medical

  • Retirement

  • PTO

Reviews contract, consent, budget, amendments, and other modifications to documentation for appropriateness. Acts as liaison between SH legal, clinical trials program and CRO/Sponsor to insure ...

Exelixis

Clinical Trials Manager (Oncology)

Alameda, CA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Manages clinical trials, including those conducted through Contract Research Organizations (CROs) May participate in developing and recommending operational strategies for clinical trials in ...

Exelixis

Clinical Trials Manager (Oncology)

Alameda, CA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Full relocation provided ESSENTIAL DUTIES AND RESPONSIBILITIES: • Manages clinical trials, including those conducted through Contract Research Organizations (CROs) • May participate in developing ...

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Showing results 1-20

All JobsContract Labcorp Clinical Trials Jobs

Contract Labcorp Clinical Trials information

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$49K

$107.3K

$189K

How much do contract labcorp clinical trials jobs pay per year?

As of Aug 14, 2026, the average yearly pay for contract labcorp clinical trials in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is the difference between Contract Labcorp Clinical Trials vs Clinical Research Associate?

AspectContract Labcorp Clinical TrialsClinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRP are commonRequires similar degrees; certifications like CCRP or CRA certification are often preferred
Work EnvironmentContract-based, often in clinical settings or labs, with project-specific durationsUsually in clinical sites or research facilities, monitoring ongoing trials
Employer & IndustryContract labs, pharmaceutical companies, CROsPharmaceutical companies, CROs, research institutions

Contract Labcorp Clinical Trials professionals focus on executing specific clinical trial projects for labs and CROs, often on a contract basis. Clinical Research Associates monitor and manage clinical trials at sites, ensuring compliance and data integrity. While both roles require similar credentials and work in related environments, their responsibilities and employment types differ.

What cities are hiring for Contract Labcorp Clinical Trials jobs?

Cities with the most Contract Labcorp Clinical Trials job openings:

What are the most commonly searched types of Labcorp Clinical Trials jobs?

The most popular types of Labcorp Clinical Trials jobs are:

What states have the most Contract Labcorp Clinical Trials jobs?

States with the most job openings for Contract Labcorp Clinical Trials jobs include:

Contract Labcorp Clinical Trials jobs near you

Clinical Trials Manager

Clinical Dynamix

Burlington, MA • On-site

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Clinical Trials Manager

The Clinical Trials Manager is responsible for the delivery of a key phase 3 clinical trial. This individual will contribute to the success of the team and organization by delivering high quality operational excellence on all delegated responsibilities while upholding our core working behaviors of Trust and Respect, Communication and Feedback, Accountability and Reliability, Objectivity, and Team Balance and Enablement.

Key Responsibilities
  • Provide strategic and operational oversight for global clinical trials.
  • Support CRO and vendor management, including governance, performance tracking, and risk mitigation.
  • Collaborate with internal functions (Regulatory, Medical, Biometrics, Pharmacovigilance, CMC, quality) to align on study plans and timelines.
  • Monitor trial progress against key deliverables (recruitment, data quality, protocol compliance, etc).
  • Review, drive essential trial documents (protocols, ICFs, plans, manuals).
  • Support country and site selection, start-up activities, and site engagement strategy.
  • Manage and support sites in study maintenance for a fast-enrolling trial
  • Ensure compliance with ICH-GCP, SOPs, and applicable regulatory requirements.
  • Support study budgets and contracts in collaboration with finance and legal teams.
  • Contribute to clinical development strategy and operational planning.
  • Prepare for and participate in study audits, inspections and data deliverables
  • Attend Site Investigator Visits and build and maintain relationships with key stakeholders.
  • Adhering to Company Standard Operating Procedures, Policies and applicable regulatory requirements
  • Execute day-to-day responsibilities of the role, ensuring quality, accuracy, and timeliness.
  • Collaborate effectively with colleagues, sharing knowledge and supporting team goals.
  • Contribute to problem-solving and decision-making processes with an objective, data-driven approach.
  • Communicate clearly and proactively with stakeholders to ensure alignment.
  • Demonstrate ownership of tasks and follow through to successful completion.
  • Support team members through constructive feedback, mentorship, and collaboration.
Skills and Qualifications
  • Bachelor's degree in life sciences, nursing, pharmacy, public health, or a related field (Advanced degree preferred but not required)
  • ~7 years in Clinical Operations or related function
  • Strong working knowledge of ICH-GCP, and experience working on global clinical trials
  • Strong interpersonal and communication skills, with the ability to adapt to different audiences.
  • Excellent organizational skills
  • Proven ability to build trust and credibility through integrity, openness, and respect.
  • Demonstrated accountability in delivering results and meeting commitments.
  • Analytical mindset with the ability to use facts and data to guide decisions.
  • Ability to work both independently and collaboratively within a team.

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