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Director Clinical Data Management Jobs in Silver Spring, MD

Ambu

Clinical Data Manager

Columbia, MD · On-site

Director, Clinical Data Acquisition Location: Remote or Columbia, MD POSITION SUMMARY Ambu is ... Support study budgets, contracts, site agreements, and vendor management in collaboration with ...

MCRA

Associate Data Manager

Washington, DC · On-site

Knowledge of clinical data management processes and GCPs preferred. * Computer literacy and ... Must be self-motivated and perform excellent work with limited direct oversight/guidance. * Ability ...

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 ...

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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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Director Clinical Data Management information

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$55.8K

$160.1K

$252.2K

How much do director clinical data management jobs pay per year?

As of Aug 15, 2026, the average yearly pay for director clinical data management in Silver Spring, MD is $160,104.00, according to ZipRecruiter salary data. Most workers in this role earn between $113,700.00 and $195,900.00 per year, depending on experience, location, and employer.

What are typical challenges faced by a director clinical data management, and how can a candidate prepare for them?

As a Director of Clinical Data Management, you may encounter challenges such as managing cross-functional teams, ensuring data integrity across complex global trials, and staying current with changing regulatory guidelines. Effective directors address these challenges through strong project management, robust communication, and fostering a culture of continuous process improvement. Candidates can prepare by gaining hands-on experience with major data management systems, keeping up with industry best practices, and developing leadership abilities to motivate diverse teams. Proactively identifying and resolving potential data issues is also key to success in this strategic role.

What is a director clinical data management?

A Director of Clinical Data Management oversees the collection, processing, and quality control of clinical trial data to ensure accuracy, compliance, and regulatory adherence. They manage data management teams, develop protocols, and implement data standards to support clinical research. This role requires expertise in regulatory guidelines (e.g., FDA, ICH-GCP), database systems, and statistical processes. The director collaborates with cross-functional teams, including biostatisticians, clinical operations, and regulatory affairs, to ensure data integrity throughout the trial lifecycle.

What are the key skills and qualifications needed to thrive as a director clinical data management?

To thrive as a Director Clinical Data Management, you need extensive experience in clinical data management, good knowledge of regulatory requirements, and usually an advanced degree in a related field. Familiarity with clinical trial data systems like EDC (Electronic Data Capture), CDISC standards, and certifications such as CCDM (Certified Clinical Data Manager) are commonly expected. Outstanding leadership, problem-solving, and communication skills help you manage teams and collaborate across departments. These competencies are crucial for ensuring high-quality, compliant data that supports successful clinical trials and regulatory submissions.

What are the most commonly searched types of Clinical Data Management jobs in Silver Spring, MD?

The most popular types of Clinical Data Management jobs in Silver Spring, MD are:

What are popular job titles related to Director Clinical Data Management jobs in Silver Spring, MD?

For Director Clinical Data Management jobs in Silver Spring, MD, the most frequently searched job titles are:

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The top searched job categories for Director Clinical Data Management jobs in Silver Spring, MD are:

What cities near Silver Spring, MD are hiring for Director Clinical Data Management jobs?

Cities near Silver Spring, MD with the most Director Clinical Data Management job openings:

Director Clinical Data Management jobs near you
Infographic showing various Director Clinical Data Management job openings in Silver Spring, MD as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, and 3% Contract. Highlights an 91% Physical, 4% Hybrid, and 5% Remote job distribution, with an average salary of $160,104 per year, or $77 per hour.

Clinical Data Manager

Ambu

Columbia, MD • On-site

Full-time

Posted 29 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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