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Greenlight Clinical Jobs (NOW HIRING)

Immatics NV

Clinical Trial Manager

$130K - $150K/yr

Lead site feasibility, selection, initiation, and greenlight activities for clinical trial sites * Develop and maintain study-specific operational plans, training materials, and monitoring ...

RecruitWell

Urology Physician

Nacogdoches, TX

... clinical and administrative staffAccess to robotic and specialty equipment: Da Vinci Xi, Greenlight Laser, and ESWLShared call rotation (1:3)Hospital ED unassigned call: 7 days per month, with ...

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All JobsGreenlight Clinical Jobs

Greenlight Clinical information

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$28

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$96

How much do greenlight clinical jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for greenlight clinical 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 is the difference between Greenlight Clinical vs Clinical Research Coordinator?

AspectGreenlight ClinicalClinical Research Coordinator
Required CredentialsBachelor's degree, relevant certifications (e.g., CCRP)Bachelor's degree, often CCRP or similar certifications
Work EnvironmentClinical trial sites, hospitals, research centersHospitals, research institutions, clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, academic medical centers, research organizations
Common Search/ComparisonGreenlight Clinical vs Clinical Research Coordinator

Greenlight Clinical and Clinical Research Coordinators both work in clinical trial settings, often requiring similar educational backgrounds and certifications. While Greenlight Clinical may focus more on specific trial management services, Clinical Research Coordinators are directly involved in patient interactions and trial coordination. Both roles are essential in the clinical research industry and share overlapping work environments and credentials.

How does a clinical research associate at Greenlight Clinical typically collaborate with investigators and study sites?

Clinical research associates (CRAs) at Greenlight Clinical play a key role in facilitating communication between the sponsor, investigators, and study sites. They regularly monitor site activities to ensure compliance with protocols and regulatory requirements, provide training and support to site staff, and resolve issues that arise during the study. CRAs often travel to different sites, review data collection processes, and participate in meetings to keep projects on track. This collaborative approach ensures the studies run smoothly and data integrity is maintained.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate at Greenlight Clinical, and why are they important?

To thrive as a Clinical Research Associate at Greenlight Clinical, you need a solid background in life sciences or healthcare, experience in clinical trials, and a relevant degree such as a BSc in a scientific discipline. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and knowledge of Good Clinical Practice (GCP) guidelines are typically required. Exceptional attention to detail, strong organizational skills, and effective communication set top performers apart in this role. These skills are crucial to ensure clinical studies are conducted efficiently, ethically, and in compliance with regulatory standards.

What is Greenlight Clinical?

Greenlight Clinical is a contract research organization (CRO) that provides clinical trial management services for pharmaceutical, biotechnology, and medical device companies. They specialize in helping sponsors design, conduct, and monitor clinical trials to ensure compliance with regulatory standards and efficient study execution. Greenlight Clinical offers support in various stages of the clinical research process, from project planning and site management to data analysis and reporting. Their expertise helps accelerate the development of new therapies and medical products.
More about Greenlight Clinical jobs
What job categories do people searching Greenlight Clinical jobs look for? The top searched job categories for Greenlight Clinical jobs are:
Greenlight Clinical jobs near you
Infographic showing various Greenlight Clinical job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 88% Full Time, and 11% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Research Coordinator

Surestep Foot & Ankle Medical Center LLC

Cincinnati, OH • On-site

$23.25 - $31/hr

Full-time

Posted 19 days ago

Job description

Cincinnati, OH (Mason Montgomery & Cheviot + surrounding areas)Position Overview

Ohio Foot & Ankle Specialists is seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to support ongoing and upcoming clinical trials in the Cincinnati region. This role is ideal for someone who thrives in a fast-paced environment, enjoys patient interaction, and is comfortable traveling between multiple clinical sites.

________________________________________

Primary Locations
  • Mason Montgomery
  • Cheviot
  • Additional surrounding locations as needed

    • ________________________________________

    Key Responsibilities
  • Coordinate and conduct clinical research study visits in accordance with protocol
  • Enter and maintain accurate data in Electronic Data Capture (EDC) systems (e.g., Greenlight Guru)
  • Identify potential study participants through EMR review based on inclusion/exclusion criteria
  • Conduct community outreach to recruit new study candidates
  • Ensure compliance with study protocols, GCP guidelines, and regulatory requirements
  • Maintain study documentation, logs, and regulatory binders
  • Manage Investigational Product (IP), including storage, accountability, and documentation
  • Transport study supplies between locations, including medical devices (e.g., Moleculight)
  • Monitor inventory and order supplies as needed

    • ________________________________________

    Travel Requirements
  • Frequent travel between sites is required
  • Mileage reimbursement provided
  • Monthly mileage submission required via expense report

    • ________________________________________

    Schedule
  • Flexible based on patient visits and study needs
  • Nonpatient days will be used for: oData entry and documentation
  • Patient recruitment efforts
  • Community outreach

    • ________________________________________

    Qualifications
  • Previous clinical research experience preferred (CRC, MA, LPN, or similar role)
  • Strong organizational and communication skills
  • Ability to work independently across multiple locations
  • Comfortable with technology and EMR systems
  • Reliable transportation required

    • ________________________________________

    What We Offer
  • Competitive compensation
  • Mileage reimbursement
  • Opportunity to grow within a rapidly expanding research program
  • Meaningful work improving patient outcomes through clinical research

    • Ohio Foot and Ankle Specialists is an Equal Opportunity Employer and considers all qualified applicants without regard to protected characteristics.

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