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Medical In Clinical Trials Jobs (NOW HIRING)

Clinical Dynamix

Clinical Trials Manager

Burlington, MA · On-site

Collaborate with internal functions (Regulatory, Medical, Biometrics, Pharmacovigilance, CMC ... Manage and support sites in study maintenance for a fast-enrolling trial * Ensure compliance with ...

New

NY SCIENTIFIC CORP

Clinical Trials Recruiter

Brooklyn, NY · On-site +1

$20 - $30/hr

About Us We are a dedicated clinical research site committed to advancing medical knowledge through ... Previous experience in patient recruitment, sales, customer service, or healthcare preferred.

Worldwide Clinical Trials Holdings, Inc.

NY · On-site

$134.50 - $267.50/hr

Company Overview Worldwide Clinical Trials is a global, midsize CRO dedicated to advancing cures ... At least 2 years of medical monitoring in clinical research or related industry * Excellent ...

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How much do medical in clinical trials jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for medical in clinical trials in the United States is $20.45, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $22.12 per hour, depending on experience, location, and employer.

What is the difference between Medical In Clinical Trials vs Clinical Research Coordinator?

AspectMedical In Clinical TrialsClinical Research Coordinator
CredentialsMedical degree or relevant healthcare certificationBachelor's degree, often in health or science fields
Work EnvironmentHospitals, clinics, research centersResearch sites, hospitals, clinics
Employer & IndustryPharmaceutical companies, CROs, academic institutionsResearch organizations, hospitals, clinics
Primary FocusOverseeing patient care and medical procedures in trialsManaging study logistics, data collection, and compliance

Medical In Clinical Trials typically involves direct patient care and medical oversight during clinical studies, requiring healthcare credentials. In contrast, Clinical Research Coordinators focus on managing study operations and data. Both roles are essential in clinical research but differ in responsibilities and qualifications.

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Medical In Clinical Trials jobs near you
Infographic showing various Medical In Clinical Trials job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $42,540 per year, or $20.5 per hour.

Clinical Trials Manager

Clinical Dynamix

Burlington, MA • On-site

Other

Posted yesterday

New

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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