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Clinical Trials Jobs (NOW HIRING)

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 ...

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Clinical Trials Recruiter

Brooklyn, NY ยท On-site +1

$20 - $30/hr

Job Title: Clinical Trials Recruiter Location: Brooklyn, NY / [On-site and Remote] Compensation: based on experience Job Type: [Part-time but potential to become full-time]. About Us We are a ...

Clinical Trials Recruiter

Brooklyn, NY ยท On-site +1

$20 - $30/hr

Job Title: Clinical Trials Recruiter Location: Brooklyn, NY / [On-site and Remote] Compensation: based on experience Job Type: [Part-time but potential to become full-time]. About Us We are a ...

Clinical Trials Recruiter

Brooklyn, NY ยท On-site

$20 - $30/hr

Clinical Trials Recruiter Location: Brooklyn, NY / [On-site and Remote] Compensation: based on experience Job Type: [Part-time but potential to become full-time]. About Us We are a dedicated clinical ...

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Clinical Trials information

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How much do clinical trials jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for clinical trials in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in a clinical trials position, and why are they important?

To thrive in Clinical Trials roles, you need a strong understanding of clinical research principles, Good Clinical Practice (GCP) guidelines, and a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and relevant certifications such as GCP or CCRA is highly valuable. Attention to detail, organizational skills, and effective communication enable collaboration across multidisciplinary teams. These competencies are crucial for ensuring protocol adherence, data integrity, and the successful execution of trial activities.

What are some common career paths or advancement opportunities for professionals working in clinical trials?

Many professionals in Clinical Trials start their careers as Clinical Research Coordinators, Clinical Research Associates, or Data Managers. With experience, you can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Project Manager, and potentially move into areas like regulatory affairs, medical writing, or quality assurance. The role offers continuous learning opportunities, exposure to innovative therapies, and often provides the chance to lead larger, more complex studies as you progress. Advancement is typically supported by additional certifications, strong performance, and a proactive approach to professional development. Teamwork and networking within the industry can also open new doors for growth.

What is a clinical trial?

A Clinical Trials job involves managing, coordinating, or supporting research studies that evaluate the safety and effectiveness of medical treatments, drugs, or devices. Professionals in this field work on trial design, patient recruitment, data collection, regulatory compliance, and reporting results. Roles can range from clinical research coordinators to trial managers and regulatory specialists. The goal is to ensure that studies follow ethical guidelines and produce reliable data for medical advancements.

What cities are hiring for Clinical Trials jobs? Cities with the most Clinical Trials job openings:
What are the most commonly searched types of Clinical Trials jobs? The most popular types of Clinical Trials jobs are:
What states have the most Clinical Trials jobs? States with the most job openings for Clinical Trials jobs include:
Infographic showing various Clinical Trials job openings in the United States as of August 2026, with employment types broken down into 17% As Needed, and 83% Full Time. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trials Manager

Clinical Dynamix

Burlington, MA โ€ข On-site

Other

Posted yesterday

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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.