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Clinical Trial Rn Jobs in Maryland (NOW HIRING)

Ambu

Clinical Trial Manager

Columbia, MD · On-site

Bachelor's degree in Life Sciences, Nursing, Biomedical Engineering, or another relevant scientific discipline. * Several years of clinical operations or clinical trial management experience within ...

Axle

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Nursing Software * Experience with clinical trial management systems and research database Skills * Experience with technology transfer agreements, clinical trial agreements, cooperative research and ...

GAP SOLUTIONS INC

Registered Nurse (51935)

Rockville, MD · On-site

$82 - $102/hr

Provide expertise in clinical trial coordination and management of data acquisition. * Review ... MD, RN, PA, or NP (practicing license not necessary) * Experienced in Current Good Clinical ...

New

Guidehouse

Clinical Program Manager

Bethesda, MD · On-site

$85K - $141K/yr

Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust ... Master's degree in health and medical administrative services, nursing, or a related field.

Guidehouse

Clinical Program Manager

Bethesda, MD · On-site

$85K - $141K/yr

Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust ... Master's degree in health and medical administrative services, nursing, or a related field.

Medix

Oncology Registered Nurse

Bethesda, MD · On-site

$45 - $52/hr

Monitor patient status and side effects related to radiation therapy and ongoing clinical trial ... Active, unrestricted Registered Nurse (RN) license; current BLS certification. Skills * Technical ...

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Clinical Trial Rn information

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$27

$60

$93

How much do clinical trial rn jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical trial rn in Maryland is $60.67, according to ZipRecruiter salary data. Most workers in this role earn between $49.23 and $68.37 per hour, depending on experience, location, and employer.

What is a Clinical Trial RN?

A Clinical Trial RN (Registered Nurse) is a specialized nurse who plays a key role in clinical research studies. They assist in patient recruitment, administer treatments, monitor patient responses, and ensure adherence to study protocols. They also collect and document data, work closely with principal investigators, and ensure compliance with regulatory guidelines. Their role is essential in advancing medical research and improving patient care through clinical trials.

What are the typical responsibilities of a Clinical Trial RN?

As a Clinical Trial RN, your daily tasks often involve screening and enrolling study participants, administering investigational treatments, monitoring patient responses, and accurately documenting all trial data. You will collaborate closely with physicians, research coordinators, and other healthcare professionals to ensure adherence to study protocols and patient safety guidelines. Additionally, you may educate patients and their families about trial procedures and follow up with them throughout the study. This role combines patient care with administrative and regulatory responsibilities, offering a dynamic and meaningful work environment.

What are the key skills and qualifications needed to thrive as a Clinical Trial RN?

To thrive as a Clinical Trial RN, you need a solid background in nursing practice, current RN licensure, and an understanding of clinical research protocols. Familiarity with clinical trial management systems, electronic data capture tools, and Good Clinical Practice (GCP) certification is often required. Strong attention to detail, superior organizational abilities, and effective communication skills make candidates excel in this role. These competencies are crucial to ensure patient safety, regulatory compliance, and the accurate collection and reporting of trial data.

How to get into clinical trial registered nurse?

To become a clinical trial registered nurse, you typically need to hold a valid registered nurse (RN) license, gain experience in medical or research settings, and obtain specialized training in clinical research protocols. Certification through organizations like the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) can enhance job prospects. Strong communication skills, attention to detail, and familiarity with Good Clinical Practice (GCP) guidelines are also important.

What do clinical trial RNs do in clinical trials?

Clinical trial RNs coordinate and monitor patient care during clinical studies, ensuring protocol adherence and accurate data collection. They perform assessments, administer treatments, educate participants, and document outcomes while following regulatory and safety guidelines.

What are the most commonly searched types of Clinical Trial Rn jobs in Maryland?

The most popular types of Clinical Trial Rn jobs in Maryland are:

What are popular job titles related to Clinical Trial Rn jobs in Maryland?

For Clinical Trial Rn jobs in Maryland, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Rn jobs in Maryland look for?

The top searched job categories for Clinical Trial Rn jobs in Maryland are:

Clinical Trial Rn jobs near you
Infographic showing various Clinical Trial Rn job openings in Maryland as of August 2026, with employment types broken down into 89% Full Time, and 11% Part Time. Highlights an 96% In-person, and 4% Remote job distribution, with an average salary of $126,203 per year, or $60.7 per hour.

Clinical Trial Manager

Ambu

Columbia, MD • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Key responsibilities

  • Lead the planning, execution, monitoring, and close-out of clinical studies in accordance with ISO 14155, GCP, and regulatory requirements.

  • Partner with stakeholders to support protocol development, study design, and operational planning.

  • Identify, qualify, initiate, and manage clinical study sites, perform site monitoring activities, and serve as the primary operational liaison.

Job description

Clinical Trial Manager
City: Columbia, MD
Country/Region: United States
State:
Business Area: Clinical Research
Department: Clinical Affairs
Employment Type: Full-time
Req ID: 10220
Job Title: Clinical Trial Manager
Reports to: Director, Clinical Data Acquisition
Location: Remote or Columbia, MD
POSITION SUMMARY
Ambu is advancing the future of endoscopy through data-driven innovation. As part of our growing Clinical Data Acquisition team, the Clinical Trial Manager will play a critical role in generating the high-quality clinical data needed to support the development of Ambu's next generation of AI-powered Endointelligence solutions.
Unlike traditional pharmaceutical clinical trial roles, this position focuses on the planning, execution, and oversight of medical device clinical studies designed to acquire clinical data that supports product innovation, algorithm development, and clinical validation. Working cross-functionally with Clinical Affairs, R&D, Software Engineering, Regulatory Affairs, Quality, and Commercial teams, the Clinical Data Manager will manage clinical studies from planning through closeout while ensuring compliance with applicable regulatory requirements, quality standards, and study timelines. This is a highly collaborative, hands-on role with significant interaction across internal teams, clinical sites, and external partners. As part of a newly established function, this individual will also help build scalable processes and contribute to the continued growth of Ambu's clinical data capabilities.
ESSENTIAL FUNCTIONS & RESPONSIBILITIES
  • Lead the planning, execution, monitoring, and close-out of clinical studies in accordance with ISO 14155, Good Clinical Practice (GCP), and applicable regulatory requirements.
  • Partner with cross-functional stakeholders to support protocol development, study design, and operational planning.
  • Identify, qualify, initiate, and manage clinical study sites across North America and Europe, as needed.
  • Perform or oversee site monitoring activities, including coordination with Contract Research Organizations (CROs) when applicable.
  • Serve as the primary operational liaison between clinical sites, investigators, internal stakeholders, and external vendors.
  • Support study budgets, contracts, site agreements, and vendor management in collaboration with internal partners.
  • Monitor enrollment, site performance, study milestones, and overall study progress while proactively identifying and resolving operational challenges.
  • Maintain study documentation and ensure compliance with internal quality systems, regulatory standards, and applicable SOPs.
  • Contribute to the development, implementation, and continuous improvement of Clinical Operations processes and Standard Operating Procedures (SOPs).
  • Support internal and external audits and regulatory inspections as required.
  • Provide regular study status updates, risk assessments, and recommendations to project stakeholders.
  • Travel to investigator sites as needed to support study execution and monitoring activities.

QUALIFICATIONS
REQUIRED:
  • Bachelor's degree in Life Sciences, Nursing, Biomedical Engineering, or another relevant scientific discipline.
  • Several years of clinical operations or clinical trial management experience within the medical device, biotechnology, or healthcare industry.
  • Strong working knowledge of ISO 14155 and Good Clinical Practice (GCP) requirements for medical device clinical investigations.
  • Experience managing investigator sites, study monitoring, and overall clinical study execution.
  • Demonstrated ability to manage multiple studies and priorities simultaneously.
  • Strong organizational, project management, and stakeholder management skills.
  • Excellent written and verbal communication skills.
  • Ability to work effectively within a global, cross-functional organization.

PREFERRED:
  • Experience supporting AI-enabled medical technologies, digital health, imaging, or software-based medical devices.
  • Experience working with Contract Research Organizations (CROs) from either the sponsor or vendor perspective.
  • Exposure to protocol development, regulatory submissions, or clinical study design.
  • Experience supporting global or multi-center clinical studies.

WHO YOU ARE
  • You are a proactive and collaborative clinical operations professional who enjoys building new capabilities and solving complex challenges.
  • You balance strong attention to detail with the ability to see the bigger picture and thrive in dynamic, cross-functional environments.
  • Take a practical, solution-oriented approach while maintaining regulatory compliance.
  • Build trusted relationships with investigators, clinical sites, and internal stakeholders.
  • Communicate effectively across technical and non-technical teams.
  • Enjoy working in fast-paced environments where processes continue to evolve.
  • Are motivated by improving patient care through innovation and high-quality clinical data.

WHY JOIN AMBU?
This is an exciting opportunity to join a newly established team helping shape the future of AI-enabled healthcare. At Ambu, you'll have the opportunity to:
  • Help build a new clinical data acquisition function from the ground up.
  • Work at the intersection of clinical research, medical devices, software, and artificial intelligence.
  • Collaborate with global teams across Clinical Affairs, R&D, Software, Regulatory, and Commercial.
  • Make a meaningful impact on innovative technologies that improve patient care worldwide.
  • Grow your career within a global medical technology company committed to innovation and continuous improvement.

#Remote (LI)
About Ambu
Ambu has been bringing the solutions of the future to life since 1937. Today, millions of patients and healthcare professionals worldwide depend on the efficiency, safety and performance of our single-use endoscopy, anaesthesia, and patient monitoring solutions. We continuously look to the future with a commitment to deliver innovative quality products that have a positive impact on patient care and the work of healthcare professionals. Headquartered near Copenhagen in Denmark, Ambu employs approximately 4,500 people in Europe, North America and the Asia Pacific.
For more information, please visit ambu.com or follow us on LinkedIn.
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About Ambu

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

501 - 1,000 Employees

Headquarters location

Noblesville, IN, US

Year founded

1937

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