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Clinical Data Jobs in Washington (NOW HIRING)

Ambu

Clinical Data Manager

Columbia, MD · On-site

Clinical Data 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:

Peers & Partners Inc

Clinical Data Manager

Bethesda, MD · On-site

CDMs will provide comprehensive data management support to clinical research teams and contribute directly to the quality, integrity, and usability of clinical research data. In addition, CDMs will ...

Peers and Partners

Clinical Data Manager

Bethesda, MD · On-site

CDMs will provide comprehensive data management support to clinical research teams and contribute directly to the quality, integrity, and usability of clinical research data. In addition, CDMs will ...

CRi

Clinical Data & Applications Analyst II

Chantilly, VA · On-site

$65K - $70K/yr

Description Clinical Data & Applications Analyst Position Summary CRi is seeking a Clinical Data & Applications Analyst to support the management, optimization, and implementation of our clinical ...

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Clinical Data information

See Washington salary details

$22

$64

$92

How much do clinical data jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for clinical data in Washington is $64.75, according to ZipRecruiter salary data. Most workers in this role earn between $51.20 and $77.07 per hour, depending on experience, location, and employer.

What is clinical data?

Clinical data refers to information collected during the course of ongoing patient care or as part of a clinical trial program. This data includes patient demographics, medical history, lab results, imaging studies, treatment plans, and outcomes. Clinical data is crucial for informing medical decisions, improving patient care, and supporting medical research and drug development. It is typically collected and managed by healthcare providers, researchers, and data professionals while maintaining strict standards for patient privacy and data security.

What are some common challenges faced by professionals working in clinical data roles, and how can they be addressed?

Professionals in Clinical Data roles often encounter challenges such as managing large volumes of complex data, ensuring data quality and integrity, and adhering to strict regulatory standards. These challenges can be addressed by staying updated on industry best practices, utilizing advanced data management tools, and working closely with cross-functional teams such as clinical research and regulatory affairs. Continuous professional development and effective communication within the team are also key to overcoming these hurdles and ensuring successful clinical trial outcomes.

What are the key skills and qualifications needed to thrive as a clinical data specialist, and why are they important?

To thrive as a Clinical Data Specialist, you need a solid background in life sciences, data management principles, and familiarity with regulatory guidelines, often supported by a relevant degree. Proficiency in clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of standards like CDISC or MedDRA is typically required. Strong attention to detail, analytical thinking, and effective communication skills are crucial soft skills for this role. These competencies ensure the accuracy and integrity of clinical trial data, supporting regulatory compliance and reliable outcomes in clinical research.

What is the difference between Clinical Data vs Clinical Data Coordinator?

AspectClinical DataClinical Data Coordinator
CredentialsTypically requires a degree in health informatics, life sciences, or related fieldRequires similar credentials, often with additional certification in clinical research or data management
Work EnvironmentData analysis, database management, and reporting in healthcare or research settingsOversees data collection, entry, and quality control in clinical trial or healthcare environments
Employer & Industry UsageUsed across hospitals, research institutions, and pharmaceutical companiesCommonly employed in clinical research organizations and hospitals

While both roles involve handling clinical data, Clinical Data professionals focus on data analysis and management, whereas Clinical Data Coordinators oversee data collection and quality assurance in clinical trials or healthcare settings.

What are the most commonly searched types of Clinical Data jobs in Washington?

The most popular types of Clinical Data jobs in Washington are:

Clinical Data jobs near you
Infographic showing various Clinical Data job openings in Washington as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 9% Part Time, 2% Temporary, and 7% Contract. Highlights an 81% Physical, 4% Hybrid, and 15% Remote job distribution, with an average salary of $134,676 per year, or $64.7 per hour.

Clinical Data Manager

Ambu

Columbia, MD • On-site

Full-time

Re-posted 3 days ago

Job description

Clinical Data 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 Data 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 Data 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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