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Clinical Research Data Manager Jobs in Silver Spring, MD

Axle

Temporary - Clinical Research Coordinator

Baltimore, MD · On-site

$24 - $32/hr

Instruct data entry and clinical staff in procedures relative to data management, protocol ... Mentor new clinical research coordinators on all aspects of research support. Disclaimer: The above ...

Axle

Temporary - Clinical Research Coordinator

Baltimore, MD · On-site

$24 - $32/hr

Instruct data entry and clinical staff in procedures relative to data management, protocol ... Mentor new clinical research coordinators on all aspects of research support. Disclaimer: The above ...

A-Team Solutions

RESEARCH NURSE

Bethesda, MD

$100K - $135K/yr

Manage clinical research data and support data quality assurance. Required Skills/Background: * Degree from a professional nursing program approved by the legally designated State accrediting agency ...

Cape Fox Corporation

Research Nurse

Bethesda, MD · On-site

$56/hr

... management of research subject files, copying and organizing research data. * Assist in updates for clinical staff on patient care, protocol process and progress, human rights protection, ICH Good ...

Cape Fox SS

Research Nurse

Bethesda, MD · On-site

$56/hr

... management of research subject files, copying and organizing research data. Assist in updates for clinical staff on patient care, protocol process and progress, human rights protection, ICH Good ...

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All JobsClinical Research Data JobsClinical Research Data Manager JobsClinical Research Data Manager Jobs in Silver Spring, MD

Clinical Research Data Manager information

See Silver Spring, MD salary details

$50.8K

$111.2K

$195.8K

How much do clinical research data manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for clinical research data manager in Silver Spring, MD is $111,174.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,900.00 and $126,900.00 per year, depending on experience, location, and employer.

What is a clinical research data manager?

A Clinical Research Data Manager is a professional responsible for collecting, organizing, and managing the data generated during clinical trials and research studies. They ensure that the data is accurate, complete, and complies with regulatory standards. Their work is crucial for the integrity of clinical research, as it allows researchers to draw valid conclusions from the study. Data managers work closely with clinical teams, statisticians, and regulatory bodies to maintain high-quality data throughout the research process.

What are some common challenges faced by clinical research data managers during multi-site trials?

Clinical Research Data Managers often encounter challenges coordinating data collection across multiple research sites, such as ensuring consistent data entry, handling discrepancies, and maintaining data quality standards. Effective communication with site staff and timely resolution of data queries are essential to minimize delays and errors. Utilizing robust electronic data capture (EDC) systems and standardized procedures helps, but proactive problem-solving and attention to detail remain crucial for success in this role.

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

To thrive as a Clinical Research Data Manager, you need a solid background in life sciences, data management principles, and experience with clinical trial processes, often backed by a relevant bachelor's degree. Proficiency in electronic data capture (EDC) systems, database management tools like SQL, and familiarity with regulatory standards such as GCP are essential. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure data integrity and smooth collaboration across research teams. These skills are crucial for maintaining high-quality, compliant data that support successful clinical trials and regulatory submissions.

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

AspectClinical Research Data ManagerClinical Research Coordinator
Primary RoleOversees data collection, management, and quality control of clinical trial data.Coordinates daily trial activities, patient recruitment, and site management.
Required SkillsData management, database systems, regulatory compliance.Patient interaction, study protocol adherence, site coordination.
Work EnvironmentData centers, clinical trial sites, research organizations.Clinical sites, hospitals, research facilities.
Common CertificationsCDMP, SAS, or related data management certifications.GCP certification, clinical trial training.

While both roles support clinical research, the Clinical Research Data Manager focuses on data integrity and management, whereas the Clinical Research Coordinator handles trial operations and participant coordination. Understanding these differences helps in choosing the right career path or job search focus.

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

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

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

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

What job categories do people searching Clinical Research Data Manager jobs in Silver Spring, MD look for?

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

What cities near Silver Spring, MD are hiring for Clinical Research Data Manager jobs?

Cities near Silver Spring, MD with the most Clinical Research Data Manager job openings:

Clinical Research Data Manager jobs near you
Infographic showing various Clinical Research Data Manager job openings in Silver Spring, MD as of August 2026, with employment types broken down into 87% Full Time, 11% Part Time, and 2% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $111,174 per year, or $53.4 per hour.

Temporary - Clinical Research Coordinator

Axle

Baltimore, MD

$24 - $32/hr

Temporary

Medical, Dental, Vision, Retirement, PTO

Re-posted 19 days ago

Job description

(ID: 2026-2380)


Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH).


Axle is seeking a Clinical Research Coordinator (Temporary – Approximately 4 Months) to join our vibrant team at the National Institutes of Health (NIH) in Baltimore, MD. This position will support ongoing clinical research activities within the National Institute on Drug Abuse (NIDA) and offers an opportunity to contribute to cutting-edge behavioral and clinical research initiatives.


Benefits We Offer:

  • 100% Medical, Dental & Vision Coverage for Employees
  • Paid Time Off and Paid Holidays
  • 401K match up to 5%
  • Educational Benefits for Career Growth
  • Employee Referral Bonus
  • Flexible Spending Accounts:
    • Healthcare (FSA)
    • Parking Reimbursement Account (PRK)
    • Dependent Care Assistant Program (DCAP)
    • Transportation Reimbursement Account (TRN)

Position Information:

Under this task order, the contractor will independently provide support services to satisfy the overall operational objectives of the National Institute on Drug Abuse. The primary objective is to provide services and deliverables through performance of support services.

Additional Qualifications

Certifications & Licenses:

  • Minimum of one (1) year of experience in behavioral counseling, preferably in drug/smoking/alcohol treatment.

  • Minimum of three (3) years of experience in a research related field.

  • Master's degree in psychology, social work, biological sciences or related discipline.

  • Basic Life Support (BLS) certification will be required – training will be provided.

Field of Study:

  • Social Work (Required)

Software:

  • Proficient computer skills required (e.g. Microsoft Office)

Skills:

  • Will complete all NIH/NIDA Mandatory trainings or/and other required trainings by the deadline set forth.

  • Excellent analytical, organizational and time management skills required.

  • Strong communications skills, both oral and written.

  • Exceptional interpersonal skills, customer service oriented and client focused approach to work due to extensive participant contact.

  • Previous experience in human subjects' interaction (clinical or research).

  • Previous clinical trial work

Deliverables:

  • Work products and documents related to administering mental health assessments and diagnostic interviews. - Ad-Hoc

  • Work products and documents related to obtaining participant medical and drug use information according to protocol criteria. - Ad-Hoc

  • Work products and documents related to obtaining informed consent documentation from participants in the screening protocol. - Ad-Hoc

  • Work products and documents related to follow-up correspondence to candidates on recruiting status. - Ad-Hoc

  • Work products and documents related to arranging travel and distributing remuneration for candidates. - Ad-Hoc

  • Work products and documents related to scheduling phone screen scripts, in person screening appointments and communications with candidates. - Ad-Hoc

  • Work products and documents related to data entry in the electronic medical record system., generating reports; perform study procedures; process and destroy specimens as needed; maintain storage records/inventory of biological specimens. - Ad-Hoc

Statement of Work Details:

  • Assist preparing and submitting for review accurate source documents related to all research procedures . - 1
  • Participate in developing and maintaining research protocol documentation and operations. - 2
  • Assist researchers with study testing, observations data entry and other duties associated with study sessions. - 3

  • Supports clinical staff develop, implement and maintain clinical research data files and materials.

  • Acquaint participants with the MRI or mock MRI scanner to assess their comfort level, fit and eligibility to participate in MRI studies.

  • Collects research data and prepares information for inputs and analysis.

  • Verify study participant information and collect data and results of testing.

  • Assist staff develop, assemble related documentation and maintain regulatory binders for all protocols.

  • Perform accurate and timely data analysis, report results and findings and respond to sponsor queries.

  • Set up, format and enter data into spreadsheets to analyze information and create reports.

  • Enter data into research databases, systems and applications for ongoing studies.

  • Supports the development of forms and questionnaires.

  • Assist researchers develop, maintain and complete study data collection forms and source documents.

  • Review draft protocols, case report forms, and manuals of operations for clarity, and completeness.

  • Work with staff on the design, development and preparation of documents such as spreadsheets, letters, rosters, agendas, presentations and meeting minutes summaries.

  • Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.

  • Assist staff screen prospective study subjects and participate in scheduling participants for research visits and procedures.

  • Schedule and coordinate outpatient and inpatient visits, diagnostic studies and medical tests.

  • Assist researchers with the collection and analysis of research data and samples.

  • Monitors subject's progress and reports adverse events.

  • Liaison between the study subjects and the investigators concerning any problems or adverse events including out of range vitals, etc.

  • Supports assembly, development and review of new research projects.

  • Assist key research personnel ensure that clinical research activities are performed in accordance with federal, state and institutional regulations, policies and procedures.

  • Assist researchers plan and coordinate the initiation of research study protocol and the implementation of operating policies and procedures.

  • Assist researchers develop and maintain current and new research protocols.

  • Supports the creation and management of clinical websites and web-based tools.

  • Collaborate with information technology IT staff to perform updates to a variety of websites.

  • Organizes and performs clinical research, utilizing internet and other available clinical resources.

  • Maintain and organize an online resource of documentation regarding clinical trials, including Standard Operating Procedure documents for all tasks related to the handling of clinical trials.

  • Provides assistance to staff in the collection, development and quality control of essential clinical research efforts.

  • Assist staff on all facets of clinical studies including subject enrollment, scheduling outpatient appointments and inpatient admissions, travel arrangements, investigation consent, subject longitudinal monitoring, study data, sample collection and data entry.

  • Supports clinical staff develop, implement and maintain clinical research data files and materials.

  • Prepare and submit for review accurate source documents related to all research procedures.

  • Develop and maintain research protocol documentation and operations.

  • Develops and facilitates training to new research coordinators and mentors researchers in Good Clinical Practices.

  • Instruct data entry and clinical staff in procedures relative to data management, protocol instructions, Standard Operating Procedures and regulatory processes and considerations.

  • Organize, prepare and distribute informational materials and provide support to the educational mission of the study.

  • Prepare materials, coordinate scheduling, track attendance and report results of workshops related research best practices, emerging trends in clinical studies, new literature and findings and regulatory considerations.

  • Mentor new clinical research coordinators on all aspects of research support.


Disclaimer: The above description is meant to illustrate the general nature of work and level of effort being performed by individuals assigned to this position or job description. This is not restricted as a complete list of all skills, responsibilities, duties, and/or assignments required. Individuals may be required to perform duties outside of their position, job description or responsibilities as needed.


The diversity of Axle's employees is a tremendous asset. We are firmly committed to providing equal opportunity in all aspects of employment and will not tolerate any illegal discrimination or harassment based on age, race, gender, religion, national origin, disability, marital status, covered veteran status, sexual orientation, status with respect to public assistance, and other characteristics protected under state, federal, or local law and to deter those who aid, abet, or induce discrimination or coerce others to discriminate.


Accessibility: If you need an accommodation as part of the employment process please contact: careers@axleinfo.com


This role has a market-competitive salary with an anticipated base compensation range listed below. Actual salaries will vary depending on a candidate's experience, qualifications, skills, and location.

Salary Range
$60—$64 USD